ENST00000703783.1:n.554G>T
|
|
|
ENST00000703785.1:n.635G>T
|
|
|
ENST00000262464.9:c.3770G>T
MANE Select
|
ENSP00000262464.4:p.Cys1257Phe
|
|
ENST00000262464.8:c.3770G>T
|
ENSP00000262464.4:p.Cys1257Phe
|
|
ENST00000507835.5:c.320G>T
|
ENSP00000426839.1:p.Cys107Phe
|
|
ENST00000508053.5:c.3770G>T
|
ENSP00000424571.1:p.Cys1257Phe
|
|
ENST00000508989.5:c.3671G>T
|
ENSP00000425596.1:p.Cys1224Phe
|
|
ENST00000619499.4:c.3767G>T
|
ENSP00000482132.1:p.Cys1256Phe
|
|
NM_001999.3:c.3770G>T
|
NP_001990.2:p.Cys1257Phe
|
|
XM_017009228.2:c.3617G>T
|
XP_016864717.1:p.Cys1206Phe
|
|
NM_001999.4:c.3770G>T
MANE Select
|
NP_001990.2:p.Cys1257Phe
|
|