|
ENST00000313728.12:c.722-890G>T
|
ENSP00000314599.7:n.722-890G>T
|
|
|
ENST00000346817.10:c.790G>T
|
ENSP00000237865.7:p.Ala264Ser
|
|
|
ENST00000438843.6:c.*376G>T
|
ENSP00000401914.1:n.*376G>T
|
|
|
ENST00000492363.6:c.*5G>T
|
ENSP00000512459.1:n.*5G>T
|
|
|
ENST00000696199.1:c.721+4414G>T
|
ENSP00000512481.1:n.721+4414G>T
|
|
|
ENST00000286186.11:c.919G>T
MANE Select
|
ENSP00000286186.6:p.Ala307Ser
|
|
|
ENST00000272879.9:c.919G>T
|
ENSP00000272879.5:p.Ala307Ser
|
|
|
ENST00000286186.10:c.919G>T
|
ENSP00000286186.6:p.Ala307Ser
|
|
|
ENST00000313728.11:c.722-890G>T
|
ENSP00000314599.7:n.722-890G>T
|
|
|
ENST00000346817.9:c.790G>T
|
ENSP00000237865.7:p.Ala264Ser
|
|
|
ENST00000360132.7:c.*5G>T
|
ENSP00000353250.3:n.*5G>T
|
|
|
ENST00000448480.1:c.790G>T
|
ENSP00000396835.1:p.Ala264Ser
|
|
|
ENST00000492363.5:n.827G>T
|
|
|
|
NM_001206524.1:c.722-890G>T
|
NP_001193453.1:n.722-890G>T
|
|
|
NM_001206542.1:c.790G>T
|
NP_001193471.1:p.Ala264Ser
|
|
|
NM_001230.4:c.790G>T
|
NP_001221.2:p.Ala264Ser
|
|
|
NM_032974.4:c.919G>T
|
NP_116756.2:p.Ala307Ser
|
|
|
NM_032976.3:c.*5G>T
|
NP_116758.1:n.*5G>T
|
|
|
NM_032977.3:c.919G>T , LRG_33t1:c.919G>T
|
NP_116759.2:p.Ala307Ser
|
|
|
XM_005246907.2:c.916G>T
|
XP_005246964.1:p.Ala306Ser
|
|
|
XM_006712796.2:c.169G>T
|
XP_006712859.1:p.Ala57Ser
|
|
|
XM_011511990.1:c.*5G>T
|
XP_011510292.1:n.*5G>T
|
|
|
XR_923043.1:n.1123G>T
|
|
|
|
XR_923044.1:n.1031G>T
|
|
|
|
XM_006712796.3:c.169G>T
|
XP_006712859.1:p.Ala57Ser
|
|
|
XM_011511990.2:c.*5G>T
|
XP_011510292.1:n.*5G>T
|
|
|
XR_923043.2:n.1123G>T
|
|
|
|
XR_923044.2:n.1031G>T
|
|
|
|
NM_001206524.2:c.722-890G>T
|
NP_001193453.1:n.722-890G>T
|
|
|
NM_001206542.2:c.790G>T
|
NP_001193471.1:p.Ala264Ser
|
|
|
NM_001230.5:c.790G>T
|
NP_001221.2:p.Ala264Ser
|
|
|
NM_032974.5:c.919G>T
|
NP_116756.2:p.Ala307Ser
|
|
|
NM_032977.4:c.919G>T
MANE Select
|
NP_116759.2:p.Ala307Ser
|
|
|
NM_032976.4:c.*5G>T
|
NP_116758.1:n.*5G>T
|
|
