ENST00000478003.2:n.2278C>A
|
|
|
ENST00000682276.1:n.1895C>A
|
|
|
ENST00000682892.1:c.1997C>A
|
ENSP00000507214.1:p.Ser666Tyr
|
|
ENST00000682952.1:n.2089C>A
|
|
|
ENST00000684455.1:c.1663C>A
|
|
|
ENST00000684642.1:c.1847C>A
|
ENSP00000507355.1:p.Ser616Tyr
|
|
ENST00000684740.1:n.2628C>A
|
|
|
ENST00000303236.9:c.2450C>A
MANE Select
|
ENSP00000307235.3:p.Ser817Tyr
|
|
ENST00000652099.1:c.2644C>A
|
|
|
ENST00000652736.1:n.2326C>A
|
|
|
ENST00000303236.7:c.2450C>A
|
ENSP00000307235.3:p.Ser817Tyr
|
|
ENST00000415570.1:c.2087C>A
|
ENSP00000412076.1:p.Ser696Tyr
|
|
ENST00000419748.5:c.1997C>A
|
ENSP00000408325.1:p.Ser666Tyr
|
|
ENST00000470706.1:n.93C>A
|
|
|
NM_001313915.1:c.1997C>A
|
NP_001300844.1:p.Ser666Tyr
|
|
NM_004836.5:c.2450C>A
|
NP_004827.4:p.Ser817Tyr
|
|
NM_004836.6:c.2450C>A
|
NP_004827.4:p.Ser817Tyr
|
|
NR_110236.1:n.1170G>T
|
|
|
XM_005264649.3:c.1766C>A
|
XP_005264706.1:p.Ser589Tyr
|
|
XM_017005376.2:c.1766C>A
|
XP_016860865.1:p.Ser589Tyr
|
|
NM_004836.7:c.2450C>A
MANE Select
|
NP_004827.4:p.Ser817Tyr
|
|
NM_001313915.2:c.1997C>A
|
NP_001300844.1:p.Ser666Tyr
|
|