ENST00000375687.10:c.3565G>T
MANE Select
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ENSP00000364839.4:p.Ala1189Ser
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ENST00000646985.1:c.3382G>T
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ENSP00000495053.1:p.Ala1128Ser
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ENST00000647223.1:n.5918G>T
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ENST00000651418.1:c.1869+1696G>T
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ENSP00000499150.1:n.1869+1696G>T
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ENST00000306058.9:c.3550G>T
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ENSP00000305119.5:p.Ala1184Ser
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ENST00000375687.8:c.3565G>T
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ENSP00000364839.4:p.Ala1189Ser
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ENST00000613218.4:c.3565G>T
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ENSP00000480487.1:p.Ala1189Ser
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ENST00000620121.4:c.3565G>T
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ENSP00000481978.1:p.Ala1189Ser
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NM_015338.5:c.3565G>T , LRG_630t1:c.3565G>T
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NP_056153.2:p.Ala1189Ser
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XM_006723727.2:c.3562G>T
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XP_006723790.1:p.Ala1188Ser
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XM_006723728.2:c.3535G>T
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XP_006723791.1:p.Ala1179Ser
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XM_006723730.2:c.3481G>T
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XP_006723793.1:p.Ala1161Ser
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XM_006723732.2:c.3382G>T
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XP_006723795.1:p.Ala1128Ser
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XM_006723733.1:c.2881G>T
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XP_006723796.1:p.Ala961Ser
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XM_011528647.1:c.3829G>T
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XP_011526949.1:p.Ala1277Ser
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XM_011528648.1:c.3826G>T
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XP_011526950.1:p.Ala1276Ser
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XM_011528649.1:c.3745G>T
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XP_011526951.1:p.Ala1249Ser
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XM_011528650.1:c.3676G>T
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XP_011526952.1:p.Ala1226Ser
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XM_011528651.1:c.3544G>T
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XP_011526953.1:p.Ala1182Ser
|
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XM_011528652.1:c.3481G>T
|
XP_011526954.1:p.Ala1161Ser
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NM_001363734.1:c.3382G>T
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NP_001350663.1:p.Ala1128Ser
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XM_006723727.3:c.3562G>T
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XP_006723790.1:p.Ala1188Ser
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|
XM_006723728.3:c.3535G>T
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XP_006723791.1:p.Ala1179Ser
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XM_006723730.4:c.3481G>T
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XP_006723793.1:p.Ala1161Ser
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XM_011528648.3:c.3826G>T
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XP_011526950.1:p.Ala1276Ser
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XM_011528652.2:c.3481G>T
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XP_011526954.1:p.Ala1161Ser
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XM_017027704.1:c.3481G>T
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XP_016883193.1:p.Ala1161Ser
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XM_017027705.1:c.3481G>T
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XP_016883194.1:p.Ala1161Ser
|
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XM_017027706.1:c.3412G>T
|
XP_016883195.1:p.Ala1138Ser
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NM_015338.6:c.3565G>T
MANE Select
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NP_056153.2:p.Ala1189Ser
|
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