ENST00000281928.9:c.4987A>T
MANE Select
|
ENSP00000281928.3:p.Thr1663Ser
|
|
ENST00000549786.2:c.4415A>T
|
|
|
ENST00000648379.1:n.3355A>T
|
|
|
ENST00000648737.1:n.4751A>T
|
|
|
ENST00000648825.1:n.1727A>T
|
|
|
ENST00000648916.1:n.2998A>T
|
|
|
ENST00000649146.1:n.2230A>T
|
|
|
ENST00000649607.1:c.3171A>T
|
|
|
ENST00000649775.1:c.1476A>T
|
|
|
ENST00000650226.1:c.4987A>T
|
ENSP00000496981.1:p.Thr1663Ser
|
|
ENST00000281928.7:c.4987A>T
|
ENSP00000281928.3:p.Thr1663Ser
|
|
ENST00000549786.1:c.351A>T
|
|
|
ENST00000552340.1:c.19A>T
|
ENSP00000449876.1:p.Thr7Ser
|
|
NM_015335.4:c.4987A>T
|
NP_056150.1:p.Thr1663Ser
|
|
XM_011538080.1:c.4987A>T
|
XP_011536382.1:p.Thr1663Ser
|
|
XM_011538081.1:c.4984A>T
|
XP_011536383.1:p.Thr1662Ser
|
|
XM_011538082.1:c.4957A>T
|
XP_011536384.1:p.Thr1653Ser
|
|
XM_011538080.2:c.4987A>T
|
XP_011536382.1:p.Thr1663Ser
|
|
XM_011538081.2:c.4984A>T
|
XP_011536383.1:p.Thr1662Ser
|
|
XM_011538082.2:c.4957A>T
|
XP_011536384.1:p.Thr1653Ser
|
|
XM_017019090.1:c.4984A>T
|
XP_016874579.1:p.Thr1662Ser
|
|
NM_015335.5:c.4987A>T
MANE Select
|
NP_056150.1:p.Thr1663Ser
|
|