ENST00000375687.10:c.3394G>C
MANE Select
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ENSP00000364839.4:p.Glu1132Gln
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|
ENST00000646985.1:c.3211G>C
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ENSP00000495053.1:p.Glu1071Gln
|
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ENST00000647223.1:n.5747G>C
|
|
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ENST00000651418.1:c.1869+1525G>C
|
ENSP00000499150.1:n.1869+1525G>C
|
|
ENST00000306058.9:c.3379G>C
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ENSP00000305119.5:p.Glu1127Gln
|
|
ENST00000375687.8:c.3394G>C
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ENSP00000364839.4:p.Glu1132Gln
|
|
ENST00000613218.4:c.3394G>C
|
ENSP00000480487.1:p.Glu1132Gln
|
|
ENST00000620121.4:c.3394G>C
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ENSP00000481978.1:p.Glu1132Gln
|
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NM_015338.5:c.3394G>C , LRG_630t1:c.3394G>C
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NP_056153.2:p.Glu1132Gln
|
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XM_006723727.2:c.3391G>C
|
XP_006723790.1:p.Glu1131Gln
|
|
XM_006723728.2:c.3364G>C
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XP_006723791.1:p.Glu1122Gln
|
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XM_006723730.2:c.3310G>C
|
XP_006723793.1:p.Glu1104Gln
|
|
XM_006723732.2:c.3211G>C
|
XP_006723795.1:p.Glu1071Gln
|
|
XM_006723733.1:c.2710G>C
|
XP_006723796.1:p.Glu904Gln
|
|
XM_011528647.1:c.3658G>C
|
XP_011526949.1:p.Glu1220Gln
|
|
XM_011528648.1:c.3655G>C
|
XP_011526950.1:p.Glu1219Gln
|
|
XM_011528649.1:c.3574G>C
|
XP_011526951.1:p.Glu1192Gln
|
|
XM_011528650.1:c.3505G>C
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XP_011526952.1:p.Glu1169Gln
|
|
XM_011528651.1:c.3373G>C
|
XP_011526953.1:p.Glu1125Gln
|
|
XM_011528652.1:c.3310G>C
|
XP_011526954.1:p.Glu1104Gln
|
|
NM_001363734.1:c.3211G>C
|
NP_001350663.1:p.Glu1071Gln
|
|
XM_006723727.3:c.3391G>C
|
XP_006723790.1:p.Glu1131Gln
|
|
XM_006723728.3:c.3364G>C
|
XP_006723791.1:p.Glu1122Gln
|
|
XM_006723730.4:c.3310G>C
|
XP_006723793.1:p.Glu1104Gln
|
|
XM_011528648.3:c.3655G>C
|
XP_011526950.1:p.Glu1219Gln
|
|
XM_011528652.2:c.3310G>C
|
XP_011526954.1:p.Glu1104Gln
|
|
XM_017027704.1:c.3310G>C
|
XP_016883193.1:p.Glu1104Gln
|
|
XM_017027705.1:c.3310G>C
|
XP_016883194.1:p.Glu1104Gln
|
|
XM_017027706.1:c.3241G>C
|
XP_016883195.1:p.Glu1081Gln
|
|
NM_015338.6:c.3394G>C
MANE Select
|
NP_056153.2:p.Glu1132Gln
|
|