ENST00000375687.10:c.3667T>G
MANE Select
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ENSP00000364839.4:p.Ser1223Ala
|
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ENST00000646985.1:c.3484T>G
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ENSP00000495053.1:p.Ser1162Ala
|
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ENST00000647223.1:n.6020T>G
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|
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ENST00000651418.1:c.1869+1798T>G
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ENSP00000499150.1:n.1869+1798T>G
|
|
ENST00000306058.9:c.3652T>G
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ENSP00000305119.5:p.Ser1218Ala
|
|
ENST00000375687.8:c.3667T>G
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ENSP00000364839.4:p.Ser1223Ala
|
|
ENST00000613218.4:c.3667T>G
|
ENSP00000480487.1:p.Ser1223Ala
|
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ENST00000620121.4:c.3667T>G
|
ENSP00000481978.1:p.Ser1223Ala
|
|
NM_015338.5:c.3667T>G , LRG_630t1:c.3667T>G
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NP_056153.2:p.Ser1223Ala
|
|
XM_006723727.2:c.3664T>G
|
XP_006723790.1:p.Ser1222Ala
|
|
XM_006723728.2:c.3637T>G
|
XP_006723791.1:p.Ser1213Ala
|
|
XM_006723730.2:c.3583T>G
|
XP_006723793.1:p.Ser1195Ala
|
|
XM_006723732.2:c.3484T>G
|
XP_006723795.1:p.Ser1162Ala
|
|
XM_006723733.1:c.2983T>G
|
XP_006723796.1:p.Ser995Ala
|
|
XM_011528647.1:c.3931T>G
|
XP_011526949.1:p.Ser1311Ala
|
|
XM_011528648.1:c.3928T>G
|
XP_011526950.1:p.Ser1310Ala
|
|
XM_011528649.1:c.3847T>G
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XP_011526951.1:p.Ser1283Ala
|
|
XM_011528650.1:c.3778T>G
|
XP_011526952.1:p.Ser1260Ala
|
|
XM_011528651.1:c.3646T>G
|
XP_011526953.1:p.Ser1216Ala
|
|
XM_011528652.1:c.3583T>G
|
XP_011526954.1:p.Ser1195Ala
|
|
NM_001363734.1:c.3484T>G
|
NP_001350663.1:p.Ser1162Ala
|
|
XM_006723727.3:c.3664T>G
|
XP_006723790.1:p.Ser1222Ala
|
|
XM_006723728.3:c.3637T>G
|
XP_006723791.1:p.Ser1213Ala
|
|
XM_006723730.4:c.3583T>G
|
XP_006723793.1:p.Ser1195Ala
|
|
XM_011528648.3:c.3928T>G
|
XP_011526950.1:p.Ser1310Ala
|
|
XM_011528652.2:c.3583T>G
|
XP_011526954.1:p.Ser1195Ala
|
|
XM_017027704.1:c.3583T>G
|
XP_016883193.1:p.Ser1195Ala
|
|
XM_017027705.1:c.3583T>G
|
XP_016883194.1:p.Ser1195Ala
|
|
XM_017027706.1:c.3514T>G
|
XP_016883195.1:p.Ser1172Ala
|
|
NM_015338.6:c.3667T>G
MANE Select
|
NP_056153.2:p.Ser1223Ala
|
|