ENST00000325455.10:c.1954G>C
MANE Select
|
ENSP00000325120.5:p.Asp652His
|
|
ENST00000263463.9:c.1907-11137G>C
|
ENSP00000263463.5:n.1907-11137G>C
|
|
ENST00000325455.9:c.1954G>C
|
ENSP00000325120.5:p.Asp652His
|
|
ENST00000526300.5:c.1907-11137G>C
|
ENSP00000436803.1:n.1907-11137G>C
|
|
ENST00000528960.5:c.1837G>C
|
ENSP00000432914.1:p.Asp613His
|
|
ENST00000533207.5:n.1321G>C
|
|
|
ENST00000534013.5:c.172G>C
|
ENSP00000436561.1:p.Asp58His
|
|
ENST00000534780.5:c.1954G>C
|
ENSP00000432352.1:p.Asp652His
|
|
ENST00000617858.4:c.1907-11137G>C
|
ENSP00000481227.1:n.1907-11137G>C
|
|
ENST00000619228.2:c.1837G>C
|
ENSP00000482698.1:p.Asp613His
|
|
ENST00000632634.1:c.376G>C
|
ENSP00000487607.1:p.Asp126His
|
|
NM_000926.4:c.1954G>C
MANE Select
|
NP_000917.3:p.Asp652His
|
|
NM_001202474.3:c.1462G>C
|
NP_001189403.1:p.Asp488His
|
|
NM_001271161.2:c.1415-11137G>C
|
NP_001258090.1:n.1415-11137G>C
|
|
NM_001271162.1:c.172G>C
|
NP_001258091.1:p.Asp58His
|
|
NR_073141.2:n.1947G>C
|
|
|
NR_073142.2:n.1830G>C
|
|
|
NR_073143.2:n.1900-11137G>C
|
|
|
XM_006718858.2:c.1954G>C
|
XP_006718921.1:p.Asp652His
|
|
XR_947831.1:n.3526G>C
|
|
|
XM_006718858.3:c.1954G>C
|
XP_006718921.1:p.Asp652His
|
|
NM_001271162.2:c.172G>C
|
NP_001258091.1:p.Asp58His
|
|
NR_073141.3:n.1961G>C
|
|
|
NR_073142.3:n.1844G>C
|
|
|
NR_073143.3:n.1914-11137G>C
|
|
|