ENST00000367408.6:n.2483A>C
|
|
|
ENST00000367409.9:c.9196A>C
MANE Select
|
ENSP00000356379.4:p.Arg3066=
|
|
ENST00000680265.1:c.9418A>C
|
ENSP00000505384.1:p.Arg3140=
|
|
ENST00000680710.1:c.9196A>C
|
ENSP00000506676.1:p.Arg3066=
|
|
ENST00000294732.11:c.4441A>C
|
ENSP00000294732.7:p.Arg1481=
|
|
ENST00000367408.5:c.2191A>C
|
ENSP00000356378.1:p.Arg731=
|
|
ENST00000367409.8:c.9196A>C
|
ENSP00000356379.4:p.Arg3066=
|
|
ENST00000612785.1:c.3154A>C
|
ENSP00000479244.1:p.Arg1052=
|
|
NM_001206846.1:c.4441A>C
|
NP_001193775.1:p.Arg1481=
|
|
NM_018136.4:c.9196A>C
|
NP_060606.3:p.Arg3066=
|
|
NM_018136.5:c.9196A>C
MANE Select
|
NP_060606.3:p.Arg3066=
|
|
NM_001206846.2:c.4441A>C
|
NP_001193775.1:p.Arg1481=
|
|