ENST00000703783.1:n.290G>T
|
|
|
ENST00000703785.1:n.371G>T
|
|
|
ENST00000262464.9:c.3506G>T
MANE Select
|
ENSP00000262464.4:p.Cys1169Phe
|
|
ENST00000262464.8:c.3506G>T
|
ENSP00000262464.4:p.Cys1169Phe
|
|
ENST00000507835.5:c.56G>T
|
ENSP00000426839.1:p.Cys19Phe
|
|
ENST00000508053.5:c.3506G>T
|
ENSP00000424571.1:p.Cys1169Phe
|
|
ENST00000508989.5:c.3407G>T
|
ENSP00000425596.1:p.Cys1136Phe
|
|
ENST00000619499.4:c.3503G>T
|
ENSP00000482132.1:p.Cys1168Phe
|
|
NM_001999.3:c.3506G>T
|
NP_001990.2:p.Cys1169Phe
|
|
XM_017009228.2:c.3353G>T
|
XP_016864717.1:p.Cys1118Phe
|
|
NM_001999.4:c.3506G>T
MANE Select
|
NP_001990.2:p.Cys1169Phe
|
|