|
ENST00000313728.12:c.722-965C>T
|
ENSP00000314599.7:n.722-965C>T
|
|
|
ENST00000346817.10:c.715C>T
|
ENSP00000237865.7:p.His239Tyr
|
|
|
ENST00000438843.6:c.*301C>T
|
ENSP00000401914.1:n.*301C>T
|
|
|
ENST00000492363.6:c.752C>T
|
ENSP00000512459.1:p.Pro251Leu
|
|
|
ENST00000696199.1:c.721+4339C>T
|
ENSP00000512481.1:n.721+4339C>T
|
|
|
ENST00000286186.11:c.844C>T
MANE Select
|
ENSP00000286186.6:p.His282Tyr
|
|
|
ENST00000272879.9:c.844C>T
|
ENSP00000272879.5:p.His282Tyr
|
|
|
ENST00000286186.10:c.844C>T
|
ENSP00000286186.6:p.His282Tyr
|
|
|
ENST00000313728.11:c.722-965C>T
|
ENSP00000314599.7:n.722-965C>T
|
|
|
ENST00000346817.9:c.715C>T
|
ENSP00000237865.7:p.His239Tyr
|
|
|
ENST00000360132.7:c.752C>T
|
ENSP00000353250.3:p.Pro251Leu
|
|
|
ENST00000438843.5:c.*301C>T
|
ENSP00000401914.1:n.*301C>T
|
|
|
ENST00000448480.1:c.715C>T
|
ENSP00000396835.1:p.His239Tyr
|
|
|
ENST00000492363.5:n.752C>T
|
|
|
|
NM_001206524.1:c.722-965C>T
|
NP_001193453.1:n.722-965C>T
|
|
|
NM_001206542.1:c.715C>T
|
NP_001193471.1:p.His239Tyr
|
|
|
NM_001230.4:c.715C>T
|
NP_001221.2:p.His239Tyr
|
|
|
NM_032974.4:c.844C>T
|
NP_116756.2:p.His282Tyr
|
|
|
NM_032976.3:c.752C>T
|
NP_116758.1:p.Pro251Leu
|
|
|
NM_032977.3:c.844C>T , LRG_33t1:c.844C>T
|
NP_116759.2:p.His282Tyr
|
|
|
XM_005246907.2:c.841C>T
|
XP_005246964.1:p.His281Tyr
|
|
|
XM_006712796.2:c.94C>T
|
XP_006712859.1:p.His32Tyr
|
|
|
XM_011511990.1:c.749C>T
|
XP_011510292.1:p.Pro250Leu
|
|
|
XR_923043.1:n.1048C>T
|
|
|
|
XR_923044.1:n.956C>T
|
|
|
|
XM_006712796.3:c.94C>T
|
XP_006712859.1:p.His32Tyr
|
|
|
XM_011511990.2:c.749C>T
|
XP_011510292.1:p.Pro250Leu
|
|
|
XR_923043.2:n.1048C>T
|
|
|
|
XR_923044.2:n.956C>T
|
|
|
|
NM_001206524.2:c.722-965C>T
|
NP_001193453.1:n.722-965C>T
|
|
|
NM_001206542.2:c.715C>T
|
NP_001193471.1:p.His239Tyr
|
|
|
NM_001230.5:c.715C>T
|
NP_001221.2:p.His239Tyr
|
|
|
NM_032974.5:c.844C>T
|
NP_116756.2:p.His282Tyr
|
|
|
NM_032977.4:c.844C>T
MANE Select
|
NP_116759.2:p.His282Tyr
|
|
|
NM_032976.4:c.752C>T
|
NP_116758.1:p.Pro251Leu
|
|
