ENST00000325455.10:c.2063T>C
MANE Select
|
ENSP00000325120.5:p.Ile688Thr
|
|
ENST00000263463.9:c.1907-11028T>C
|
ENSP00000263463.5:n.1907-11028T>C
|
|
ENST00000325455.9:c.2063T>C
|
ENSP00000325120.5:p.Ile688Thr
|
|
ENST00000526300.5:c.1907-11028T>C
|
ENSP00000436803.1:n.1907-11028T>C
|
|
ENST00000528960.5:c.1946T>C
|
ENSP00000432914.1:p.Ile649Thr
|
|
ENST00000533207.5:n.1430T>C
|
|
|
ENST00000534013.5:c.281T>C
|
ENSP00000436561.1:p.Ile94Thr
|
|
ENST00000534780.5:c.2063T>C
|
ENSP00000432352.1:p.Ile688Thr
|
|
ENST00000617858.4:c.1907-11028T>C
|
ENSP00000481227.1:n.1907-11028T>C
|
|
ENST00000619228.2:c.1946T>C
|
ENSP00000482698.1:p.Ile649Thr
|
|
ENST00000632634.1:c.485T>C
|
ENSP00000487607.1:p.Ile162Thr
|
|
NM_000926.4:c.2063T>C
MANE Select
|
NP_000917.3:p.Ile688Thr
|
|
NM_001202474.3:c.1571T>C
|
NP_001189403.1:p.Ile524Thr
|
|
NM_001271161.2:c.1415-11028T>C
|
NP_001258090.1:n.1415-11028T>C
|
|
NM_001271162.1:c.281T>C
|
NP_001258091.1:p.Ile94Thr
|
|
NR_073141.2:n.2056T>C
|
|
|
NR_073142.2:n.1939T>C
|
|
|
NR_073143.2:n.1900-11028T>C
|
|
|
XM_006718858.2:c.2063T>C
|
XP_006718921.1:p.Ile688Thr
|
|
XR_947831.1:n.3635T>C
|
|
|
XM_006718858.3:c.2063T>C
|
XP_006718921.1:p.Ile688Thr
|
|
NM_001271162.2:c.281T>C
|
NP_001258091.1:p.Ile94Thr
|
|
NR_073141.3:n.2070T>C
|
|
|
NR_073142.3:n.1953T>C
|
|
|
NR_073143.3:n.1914-11028T>C
|
|
|