ENST00000703783.1:n.161G>C
|
|
|
ENST00000703785.1:n.242G>C
|
|
|
ENST00000262464.9:c.3377G>C
MANE Select
|
ENSP00000262464.4:p.Cys1126Ser
|
|
ENST00000262464.8:c.3377G>C
|
ENSP00000262464.4:p.Cys1126Ser
|
|
ENST00000507835.5:c.-74G>C
|
ENSP00000426839.1:n.-74G>C
|
|
ENST00000508053.5:c.3377G>C
|
ENSP00000424571.1:p.Cys1126Ser
|
|
ENST00000508989.5:c.3278G>C
|
ENSP00000425596.1:p.Cys1093Ser
|
|
ENST00000619499.4:c.3374G>C
|
ENSP00000482132.1:p.Cys1125Ser
|
|
NM_001999.3:c.3377G>C
|
NP_001990.2:p.Cys1126Ser
|
|
XM_017009228.2:c.3224G>C
|
XP_016864717.1:p.Cys1075Ser
|
|
NM_001999.4:c.3377G>C
MANE Select
|
NP_001990.2:p.Cys1126Ser
|
|