ENST00000703783.1:n.337T>G
|
|
|
ENST00000703785.1:n.418T>G
|
|
|
ENST00000262464.9:c.3553T>G
MANE Select
|
ENSP00000262464.4:p.Cys1185Gly
|
|
ENST00000262464.8:c.3553T>G
|
ENSP00000262464.4:p.Cys1185Gly
|
|
ENST00000507835.5:c.103T>G
|
ENSP00000426839.1:p.Cys35Gly
|
|
ENST00000508053.5:c.3553T>G
|
ENSP00000424571.1:p.Cys1185Gly
|
|
ENST00000508989.5:c.3454T>G
|
ENSP00000425596.1:p.Cys1152Gly
|
|
ENST00000619499.4:c.3550T>G
|
ENSP00000482132.1:p.Cys1184Gly
|
|
NM_001999.3:c.3553T>G
|
NP_001990.2:p.Cys1185Gly
|
|
XM_017009228.2:c.3400T>G
|
XP_016864717.1:p.Cys1134Gly
|
|
NM_001999.4:c.3553T>G
MANE Select
|
NP_001990.2:p.Cys1185Gly
|
|