ENST00000478003.2:n.2233C>T
|
|
|
ENST00000682276.1:n.1850C>T
|
|
|
ENST00000682892.1:c.1952C>T
|
ENSP00000507214.1:p.Thr651Ile
|
|
ENST00000682952.1:n.2044C>T
|
|
|
ENST00000684455.1:c.1618C>T
|
|
|
ENST00000684642.1:c.1802C>T
|
ENSP00000507355.1:p.Thr601Ile
|
|
ENST00000684740.1:n.2583C>T
|
|
|
ENST00000303236.9:c.2405C>T
MANE Select
|
ENSP00000307235.3:p.Thr802Ile
|
|
ENST00000652099.1:c.2599C>T
|
|
|
ENST00000652736.1:n.2281C>T
|
|
|
ENST00000303236.7:c.2405C>T
|
ENSP00000307235.3:p.Thr802Ile
|
|
ENST00000415570.1:c.2042C>T
|
ENSP00000412076.1:p.Thr681Ile
|
|
ENST00000419748.5:c.1952C>T
|
ENSP00000408325.1:p.Thr651Ile
|
|
ENST00000470706.1:n.49-1C>T
|
|
|
NM_001313915.1:c.1952C>T
|
NP_001300844.1:p.Thr651Ile
|
|
NM_004836.5:c.2405C>T
|
NP_004827.4:p.Thr802Ile
|
|
NM_004836.6:c.2405C>T
|
NP_004827.4:p.Thr802Ile
|
|
NR_110236.1:n.1215G>A
|
|
|
XM_005264649.3:c.1721C>T
|
XP_005264706.1:p.Thr574Ile
|
|
XM_017005376.2:c.1721C>T
|
XP_016860865.1:p.Thr574Ile
|
|
NM_004836.7:c.2405C>T
MANE Select
|
NP_004827.4:p.Thr802Ile
|
|
NM_001313915.2:c.1952C>T
|
NP_001300844.1:p.Thr651Ile
|
|