ENST00000325455.10:c.2241G>C
MANE Select
|
ENSP00000325120.5:p.Gln747His
|
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ENST00000263463.9:c.1935G>C
|
ENSP00000263463.5:p.Gln645His
|
|
ENST00000325455.9:c.2241G>C
|
ENSP00000325120.5:p.Gln747His
|
|
ENST00000526300.5:c.1935G>C
|
ENSP00000436803.1:p.Gln645His
|
|
ENST00000528960.5:c.2124G>C
|
ENSP00000432914.1:p.Gln708His
|
|
ENST00000533207.5:n.1608G>C
|
|
|
ENST00000534013.5:c.459G>C
|
ENSP00000436561.1:p.Gln153His
|
|
ENST00000534780.5:c.2241G>C
|
ENSP00000432352.1:p.Gln747His
|
|
ENST00000617858.4:c.1935G>C
|
ENSP00000481227.1:p.Gln645His
|
|
ENST00000619228.2:c.2124G>C
|
ENSP00000482698.1:p.Gln708His
|
|
NM_000926.4:c.2241G>C
MANE Select
|
NP_000917.3:p.Gln747His
|
|
NM_001202474.3:c.1749G>C
|
NP_001189403.1:p.Gln583His
|
|
NM_001271161.2:c.1443G>C
|
NP_001258090.1:p.Gln481His
|
|
NM_001271162.1:c.459G>C
|
NP_001258091.1:p.Gln153His
|
|
NR_073141.2:n.2234G>C
|
|
|
NR_073142.2:n.2117G>C
|
|
|
NR_073143.2:n.1928G>C
|
|
|
XM_006718858.2:c.2241G>C
|
XP_006718921.1:p.Gln747His
|
|
XR_947831.1:n.3922G>C
|
|
|
XM_006718858.3:c.2241G>C
|
XP_006718921.1:p.Gln747His
|
|
NM_001271162.2:c.459G>C
|
NP_001258091.1:p.Gln153His
|
|
NR_073141.3:n.2248G>C
|
|
|
NR_073142.3:n.2131G>C
|
|
|
NR_073143.3:n.1942G>C
|
|
|