ENST00000703783.1:n.896G>C
|
|
|
ENST00000703785.1:n.977G>C
|
|
|
ENST00000262464.9:c.4112G>C
MANE Select
|
ENSP00000262464.4:p.Cys1371Ser
|
|
ENST00000262464.8:c.4112G>C
|
ENSP00000262464.4:p.Cys1371Ser
|
|
ENST00000507835.5:c.662G>C
|
ENSP00000426839.1:p.Cys221Ser
|
|
ENST00000508053.5:c.4112G>C
|
ENSP00000424571.1:p.Cys1371Ser
|
|
ENST00000508989.5:c.4013G>C
|
ENSP00000425596.1:p.Cys1338Ser
|
|
ENST00000619499.4:c.4109G>C
|
ENSP00000482132.1:p.Cys1370Ser
|
|
NM_001999.3:c.4112G>C
|
NP_001990.2:p.Cys1371Ser
|
|
XM_017009228.2:c.3959G>C
|
XP_016864717.1:p.Cys1320Ser
|
|
NM_001999.4:c.4112G>C
MANE Select
|
NP_001990.2:p.Cys1371Ser
|
|