ENST00000703783.1:n.449C>G
|
|
|
ENST00000703785.1:n.530C>G
|
|
|
ENST00000262464.9:c.3665C>G
MANE Select
|
ENSP00000262464.4:p.Thr1222Ser
|
|
ENST00000262464.8:c.3665C>G
|
ENSP00000262464.4:p.Thr1222Ser
|
|
ENST00000507835.5:c.215C>G
|
ENSP00000426839.1:p.Thr72Ser
|
|
ENST00000508053.5:c.3665C>G
|
ENSP00000424571.1:p.Thr1222Ser
|
|
ENST00000508989.5:c.3566C>G
|
ENSP00000425596.1:p.Thr1189Ser
|
|
ENST00000619499.4:c.3662C>G
|
ENSP00000482132.1:p.Thr1221Ser
|
|
NM_001999.3:c.3665C>G
|
NP_001990.2:p.Thr1222Ser
|
|
XM_017009228.2:c.3512C>G
|
XP_016864717.1:p.Thr1171Ser
|
|
NM_001999.4:c.3665C>G
MANE Select
|
NP_001990.2:p.Thr1222Ser
|
|