ENST00000358552.8:c.961C>A
|
ENSP00000351354.5:p.Arg321=
|
|
ENST00000622520.2:c.1075+2953C>A
|
ENSP00000481181.2:n.1075+2953C>A
|
|
ENST00000693124.1:c.773+6017C>A
|
|
|
ENST00000592199.6:c.1087C>A
MANE Select
|
ENSP00000467512.1:p.Arg363=
|
|
ENST00000676441.1:c.1111C>A
|
ENSP00000502554.1:p.Arg371=
|
|
ENST00000358552.7:c.973C>A
|
ENSP00000351354.4:p.Arg325=
|
|
ENST00000360105.8:c.973C>A
|
ENSP00000353219.4:p.Arg325=
|
|
ENST00000397661.6:c.1087C>A
|
ENSP00000380781.2:p.Arg363=
|
|
ENST00000585382.5:c.*456C>A
|
ENSP00000466605.1:n.*456C>A
|
|
ENST00000585575.5:c.1063C>A
|
ENSP00000468794.1:p.Arg355=
|
|
ENST00000586797.5:c.*918C>A
|
ENSP00000467536.1:n.*918C>A
|
|
ENST00000587260.1:c.1084C>A
|
ENSP00000467785.1:p.Arg362=
|
|
ENST00000587760.5:c.1063C>A
|
ENSP00000466389.1:p.Arg355=
|
|
ENST00000588228.5:c.946C>A
|
ENSP00000466735.1:p.Arg316=
|
|
ENST00000592199.5:c.1087C>A
|
ENSP00000467512.1:p.Arg363=
|
|
NM_001271043.2:c.1111C>A
|
NP_001257972.1:p.Arg371=
|
|
NM_001271044.2:c.1063C>A
|
NP_001257973.1:p.Arg355=
|
|
NM_002501.3:c.1087C>A
|
NP_002492.2:p.Arg363=
|
|
XM_005259917.3:c.1141C>A
|
XP_005259974.1:p.Arg381=
|
|
XM_005259918.3:c.1087C>A
|
XP_005259975.1:p.Arg363=
|
|
XM_005259919.3:c.1264C>A
|
XP_005259976.1:p.Arg422=
|
|
XM_005259920.3:c.1063C>A
|
XP_005259977.1:p.Arg355=
|
|
XM_005259921.3:c.1255+2953C>A
|
XP_005259978.1:n.1255+2953C>A
|
|
XM_005259922.3:c.1132+6017C>A
|
XP_005259979.1:n.1132+6017C>A
|
|
XM_006722760.2:c.1141C>A
|
XP_006722823.1:p.Arg381=
|
|
XM_011528040.1:c.1135C>A
|
XP_011526342.1:p.Arg379=
|
|
NM_001365902.1:c.1087C>A
|
NP_001352831.1:p.Arg363=
|
|
NM_001365982.1:c.964C>A
|
NP_001352911.1:p.Arg322=
|
|
NM_001365983.1:c.946C>A
|
NP_001352912.1:p.Arg316=
|
|
NM_001365984.1:c.1084C>A
|
NP_001352913.1:p.Arg362=
|
|
NM_001365985.1:c.1084C>A
|
NP_001352914.1:p.Arg362=
|
|
XM_005259917.4:c.1141C>A
|
XP_005259974.1:p.Arg381=
|
|
NM_001271044.3:c.1063C>A
|
NP_001257973.1:p.Arg355=
|
|
NM_001365902.2:c.1087C>A
|
NP_001352831.1:p.Arg363=
|
|
NM_001365982.2:c.964C>A
|
NP_001352911.1:p.Arg322=
|
|
NM_001365983.2:c.946C>A
|
NP_001352912.1:p.Arg316=
|
|
NM_001365984.2:c.1084C>A
|
NP_001352913.1:p.Arg362=
|
|
NM_001365985.2:c.1084C>A
|
NP_001352914.1:p.Arg362=
|
|
NM_002501.4:c.1087C>A
|
NP_002492.2:p.Arg363=
|
|
NM_001365902.3:c.1087C>A
MANE Select
|
NP_001352831.1:p.Arg363=
|
|
NM_001378404.1:c.1063C>A
|
NP_001365333.1:p.Arg355=
|
|
NM_001378405.1:c.1135C>A
|
NP_001365334.1:p.Arg379=
|
|