ENST00000478003.2:n.2280A=
|
|
|
ENST00000682276.1:n.1897A=
|
|
|
ENST00000682892.1:c.1999A=
|
ENSP00000507214.1:p.Ser667=
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ENST00000682952.1:n.2091A=
|
|
|
ENST00000684455.1:c.1665A=
|
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ENST00000684642.1:c.1849A=
|
ENSP00000507355.1:p.Ser617=
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ENST00000684740.1:n.2630A=
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|
ENST00000303236.9:c.2452A=
MANE Select
|
ENSP00000307235.3:p.Ser818=
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ENST00000652099.1:c.2646A=
|
|
|
ENST00000652736.1:n.2328A=
|
|
|
ENST00000303236.7:c.2452A=
|
ENSP00000307235.3:p.Ser818=
|
|
ENST00000415570.1:c.2089A=
|
ENSP00000412076.1:p.Ser697=
|
|
ENST00000419748.5:c.1999A=
|
ENSP00000408325.1:p.Ser667=
|
|
ENST00000470706.1:n.95A=
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|
NM_001313915.1:c.1999A=
|
NP_001300844.1:p.Ser667=
|
|
NM_004836.5:c.2452A=
|
NP_004827.4:p.Ser818=
|
|
NM_004836.6:c.2452A=
|
NP_004827.4:p.Ser818=
|
|
NR_110236.1:n.1168T=
|
|
|
XM_005264649.3:c.1768A=
|
XP_005264706.1:p.Ser590=
|
|
XM_017005376.2:c.1768A=
|
XP_016860865.1:p.Ser590=
|
|
NM_004836.7:c.2452A=
MANE Select
|
NP_004827.4:p.Ser818=
|
|
NM_001313915.2:c.1999A=
|
NP_001300844.1:p.Ser667=
|
|