ENST00000478003.2:n.2211T>A
|
|
|
ENST00000682276.1:n.1828T>A
|
|
|
ENST00000682892.1:c.1930T>A
|
ENSP00000507214.1:p.Tyr644Asn
|
|
ENST00000682952.1:n.2022T>A
|
|
|
ENST00000684455.1:c.1596T>A
|
|
|
ENST00000684642.1:c.1780T>A
|
ENSP00000507355.1:p.Tyr594Asn
|
|
ENST00000684740.1:n.2561T>A
|
|
|
ENST00000303236.9:c.2383T>A
MANE Select
|
ENSP00000307235.3:p.Tyr795Asn
|
|
ENST00000652099.1:c.2577T>A
|
|
|
ENST00000652736.1:n.2259T>A
|
|
|
ENST00000303236.7:c.2383T>A
|
ENSP00000307235.3:p.Tyr795Asn
|
|
ENST00000415570.1:c.2020T>A
|
ENSP00000412076.1:p.Tyr674Asn
|
|
ENST00000419748.5:c.1930T>A
|
ENSP00000408325.1:p.Tyr644Asn
|
|
ENST00000470706.1:n.49-23T>A
|
|
|
NM_001313915.1:c.1930T>A
|
NP_001300844.1:p.Tyr644Asn
|
|
NM_004836.5:c.2383T>A
|
NP_004827.4:p.Tyr795Asn
|
|
NM_004836.6:c.2383T>A
|
NP_004827.4:p.Tyr795Asn
|
|
NR_110236.1:n.1237A>T
|
|
|
XM_005264649.3:c.1699T>A
|
XP_005264706.1:p.Tyr567Asn
|
|
XM_017005376.2:c.1699T>A
|
XP_016860865.1:p.Tyr567Asn
|
|
NM_004836.7:c.2383T>A
MANE Select
|
NP_004827.4:p.Tyr795Asn
|
|
NM_001313915.2:c.1930T>A
|
NP_001300844.1:p.Tyr644Asn
|
|