ENST00000281405.9:c.95G>T
MANE Select
|
ENSP00000281405.5:p.Gly32Val
|
|
ENST00000345530.8:c.95G>T
MANE Plus Clinical
|
ENSP00000314444.5:p.Gly32Val
|
|
ENST00000281405.8:c.95G>T
|
ENSP00000281405.4:p.Gly32Val
|
|
ENST00000345530.7:c.95G>T
|
ENSP00000314444.5:p.Gly32Val
|
|
ENST00000414212.5:c.95G>T
|
ENSP00000390802.1:p.Gly32Val
|
|
NM_001006657.1:c.95G>T
|
NP_001006658.1:p.Gly32Val
|
|
NM_020779.3:c.95G>T
|
NP_065830.2:p.Gly32Val
|
|
XR_426989.2:n.128G>T
|
|
|
XR_939699.1:n.128G>T
|
|
|
XR_001738862.1:n.128G>T
|
|
|
XR_426989.3:n.128G>T
|
|
|
XR_939699.3:n.128G>T
|
|
|
NM_001006657.2:c.95G>T
MANE Plus Clinical
|
NP_001006658.1:p.Gly32Val
|
|
NM_020779.4:c.95G>T
MANE Select
|
NP_065830.2:p.Gly32Val
|
|