ENST00000478003.2:n.1955T=
|
|
|
ENST00000682276.1:n.1572T=
|
|
|
ENST00000682892.1:c.1674T=
|
ENSP00000507214.1:p.Ile558=
|
|
ENST00000682952.1:n.1766T=
|
|
|
ENST00000684455.1:c.1340T=
|
|
|
ENST00000684642.1:c.1524T=
|
ENSP00000507355.1:p.Ile508=
|
|
ENST00000684740.1:n.2305T=
|
|
|
ENST00000303236.9:c.2127T=
MANE Select
|
ENSP00000307235.3:p.Ile709=
|
|
ENST00000652099.1:c.2321T=
|
|
|
ENST00000652736.1:n.2003T=
|
|
|
ENST00000303236.7:c.2127T=
|
ENSP00000307235.3:p.Ile709=
|
|
ENST00000415570.1:c.1764T=
|
ENSP00000412076.1:p.Ile588=
|
|
ENST00000419748.5:c.1674T=
|
ENSP00000408325.1:p.Ile558=
|
|
ENST00000470706.1:n.48+5T=
|
|
|
NM_001313915.1:c.1674T=
|
NP_001300844.1:p.Ile558=
|
|
NM_004836.5:c.2127T=
|
NP_004827.4:p.Ile709=
|
|
NM_004836.6:c.2127T=
|
NP_004827.4:p.Ile709=
|
|
NR_110236.1:n.1493A=
|
|
|
XM_005264649.3:c.1443T=
|
XP_005264706.1:p.Ile481=
|
|
XR_939749.1:n.2406T=
|
|
|
XM_017005376.2:c.1443T=
|
XP_016860865.1:p.Ile481=
|
|
NM_004836.7:c.2127T=
MANE Select
|
NP_004827.4:p.Ile709=
|
|
NM_001313915.2:c.1674T=
|
NP_001300844.1:p.Ile558=
|
|