ENST00000466617.6:c.2363C>G
|
ENSP00000420082.2:p.Ala788Gly
|
|
ENST00000470367.2:c.2651C>G
|
ENSP00000514541.1:p.Ala884Gly
|
|
ENST00000483566.2:c.2363C>G
|
ENSP00000420252.2:p.Ala788Gly
|
|
ENST00000699714.1:c.2363C>G
|
ENSP00000514539.1:p.Ala788Gly
|
|
ENST00000699715.1:c.2363C>G
|
ENSP00000514540.1:p.Ala788Gly
|
|
ENST00000699716.1:c.2363C>G
|
ENSP00000514542.1:p.Ala788Gly
|
|
ENST00000699717.1:n.2089C>G
|
|
|
ENST00000699718.1:c.3761C>G
|
ENSP00000514543.1:p.Ala1254Gly
|
|
ENST00000462833.6:c.3686C>G
MANE Select
|
ENSP00000419361.1:p.Ala1229Gly
|
|
ENST00000309879.9:c.2636C>G
|
ENSP00000308685.5:p.Ala879Gly
|
|
ENST00000462833.5:c.3686C>G
|
ENSP00000419361.1:p.Ala1229Gly
|
|
ENST00000478092.1:n.456C>G
|
|
|
ENST00000491190.5:c.2660C>G
|
ENSP00000418537.1:p.Ala887Gly
|
|
NM_001199642.1:c.2636C>G
|
NP_001186571.1:p.Ala879Gly
|
|
NM_183357.2:c.3686C>G
|
NP_899200.1:p.Ala1229Gly
|
|
XM_005247077.2:c.3761C>G
|
XP_005247134.1:p.Ala1254Gly
|
|
XM_005247078.1:c.2711C>G
|
XP_005247135.1:p.Ala904Gly
|
|
XM_006713483.1:c.2660C>G
|
XP_006713546.1:p.Ala887Gly
|
|
XM_006713484.1:c.2438C>G
|
XP_006713547.1:p.Ala813Gly
|
|
XM_011512359.1:c.2762C>G
|
XP_011510661.1:p.Ala921Gly
|
|
XM_011512360.1:c.2672C>G
|
XP_011510662.1:p.Ala891Gly
|
|
XM_011512361.1:c.2438C>G
|
XP_011510663.1:p.Ala813Gly
|
|
XM_005247077.4:c.3761C>G
|
XP_005247134.1:p.Ala1254Gly
|
|
XM_011512359.2:c.2762C>G
|
XP_011510661.1:p.Ala921Gly
|
|
XM_011512360.3:c.2672C>G
|
XP_011510662.1:p.Ala891Gly
|
|
XM_017005638.1:c.2663C>G
|
XP_016861127.1:p.Ala888Gly
|
|
XM_017005639.1:c.2663C>G
|
XP_016861128.1:p.Ala888Gly
|
|
NM_001378259.1:c.3761C>G
|
NP_001365188.1:p.Ala1254Gly
|
|
NM_183357.3:c.3686C>G
MANE Select
|
NP_899200.1:p.Ala1229Gly
|
|