ENST00000339364.10:c.2273G>A
MANE Select
|
ENSP00000339826.5:p.Arg758His
|
|
ENST00000339364.9:c.2273G>A
|
ENSP00000339826.5:p.Arg758His
|
|
ENST00000371109.3:c.1070G>A
|
ENSP00000360150.3:p.Arg357His
|
|
ENST00000371110.6:c.1739G>A
|
ENSP00000360151.2:p.Arg580His
|
|
ENST00000467625.5:n.470G>A
|
|
|
NM_152309.2:c.2273G>A
|
NP_689522.2:p.Arg758His
|
|
XM_005269498.1:c.1739G>A
|
XP_005269555.1:p.Arg580His
|
|
XM_005269499.1:c.1739G>A
|
XP_005269556.1:p.Arg580His
|
|
XM_011539248.1:c.2241+1612G>A
|
XP_011537550.1:n.2241+1612G>A
|
|
XM_011539249.1:c.2117G>A
|
XP_011537551.1:p.Arg706His
|
|
XR_946220.1:n.1413-5309C>T
|
|
|
XR_946220.3:n.1165-5309C>T
|
|
|
NM_152309.3:c.2273G>A
MANE Select
|
NP_689522.2:p.Arg758His
|
|