ENST00000696170.1:c.*542G>T
|
ENSP00000512461.1:n.*542G>T
|
|
ENST00000696171.1:c.937G>T
|
ENSP00000512462.1:p.Ala313Ser
|
|
ENST00000378588.5:c.1033G>T
MANE Select
|
ENSP00000367851.4:p.Ala345Ser
|
|
ENST00000378588.4:c.1033G>T
|
ENSP00000367851.4:p.Ala345Ser
|
|
ENST00000465127.1:c.171+378012G>T
|
ENSP00000417050.1:n.171+378012G>T
|
|
ENST00000492288.1:n.458G>T
|
|
|
NM_000397.3:c.1033G>T , LRG_53t1:c.1033G>T
|
NP_000388.2:p.Ala345Ser
|
|
XM_011543890.1:c.727G>T
|
XP_011542192.1:p.Ala243Ser
|
|
NM_000397.4:c.1033G>T
MANE Select
|
NP_000388.2:p.Ala345Ser
|
|