ENST00000519638.3:c.237T>G
MANE Select
|
ENSP00000428112.1:p.Ser79Arg
|
|
ENST00000521993.3:n.166T>G
|
|
|
ENST00000647813.1:n.503T>G
|
|
|
ENST00000648919.1:c.237T>G
|
ENSP00000497100.1:p.Ser79Arg
|
|
ENST00000276461.9:c.237T>G
|
ENSP00000276461.5:p.Ser79Arg
|
|
ENST00000335171.10:c.237T>G
|
ENSP00000335220.6:p.Ser79Arg
|
|
ENST00000397228.6:c.237T>G
|
ENSP00000380405.2:p.Ser79Arg
|
|
ENST00000518526.5:c.108T>G
|
ENSP00000429229.1:p.Ser36Arg
|
|
ENST00000518586.5:c.237T>G
|
ENSP00000427847.1:p.Ser79Arg
|
|
ENST00000519638.1:c.237T>G
|
ENSP00000428112.1:p.Ser79Arg
|
|
ENST00000521644.5:c.237T>G
|
ENSP00000429621.1:p.Ser79Arg
|
|
ENST00000521993.2:n.130T>G
|
|
|
ENST00000523107.5:c.237T>G
|
ENSP00000473292.1:p.Ser79Arg
|
|
ENST00000523887.5:c.237T>G
|
ENSP00000429903.1:p.Ser79Arg
|
|
NM_001003790.3:c.237T>G
|
NP_001003790.1:p.Ser79Arg
|
|
NM_001003791.2:c.237T>G
|
NP_001003791.1:p.Ser79Arg
|
|
NM_007175.6:c.237T>G
|
NP_009106.1:p.Ser79Arg
|
|
XM_005273392.1:c.237T>G
|
XP_005273449.1:p.Ser79Arg
|
|
XM_006716280.1:c.-10T>G
|
XP_006716343.1:n.-10T>G
|
|
NM_001362878.1:c.237T>G
|
NP_001349807.1:p.Ser79Arg
|
|
NM_001362880.1:c.237T>G
|
NP_001349809.1:p.Ser79Arg
|
|
NM_007175.7:c.237T>G
|
NP_009106.1:p.Ser79Arg
|
|
XM_005273392.3:c.237T>G
|
XP_005273449.1:p.Ser79Arg
|
|
XM_006716280.2:c.-10T>G
|
XP_006716343.1:n.-10T>G
|
|
XM_017013000.1:c.237T>G
|
XP_016868489.1:p.Ser79Arg
|
|
XM_024447058.1:c.237T>G
|
XP_024302826.1:p.Ser79Arg
|
|
NM_001003790.4:c.237T>G
|
NP_001003790.1:p.Ser79Arg
|
|
NM_001003791.3:c.237T>G
|
NP_001003791.1:p.Ser79Arg
|
|
NM_001362878.2:c.237T>G
|
NP_001349807.1:p.Ser79Arg
|
|
NM_001362880.2:c.237T>G
|
NP_001349809.1:p.Ser79Arg
|
|
NM_007175.8:c.237T>G
MANE Select
|
NP_009106.1:p.Ser79Arg
|
|