ENST00000696809.1:c.*457G>T
|
ENSP00000512887.1:n.*457G>T
|
|
ENST00000699276.1:c.1862G>T
|
ENSP00000514257.1:p.Gly621Val
|
|
ENST00000323584.10:c.1883G>T
MANE Select
|
ENSP00000313504.5:p.Gly628Val
|
|
ENST00000299167.12:c.1883G>T
|
ENSP00000299167.8:p.Gly628Val
|
|
ENST00000323584.9:c.1883G>T
|
ENSP00000313504.5:p.Gly628Val
|
|
ENST00000566044.5:c.1862G>T
|
ENSP00000456729.1:p.Gly621Val
|
|
ENST00000568171.1:n.4G>T
|
|
|
NM_000293.2:c.1883G>T
|
NP_000284.1:p.Gly628Val
|
|
NM_001031835.2:c.1862G>T
|
NP_001027005.1:p.Gly621Val
|
|
XM_005255983.3:c.1883G>T
|
XP_005256040.1:p.Gly628Val
|
|
XM_005255984.3:c.1862G>T
|
XP_005256041.1:p.Gly621Val
|
|
XM_011523106.1:c.1883G>T
|
XP_011521408.1:p.Gly628Val
|
|
XM_011523107.1:c.461G>T
|
XP_011521409.1:p.Gly154Val
|
|
NM_001363837.1:c.1883G>T
|
NP_001350766.1:p.Gly628Val
|
|
XM_005255983.4:c.1883G>T
|
XP_005256040.1:p.Gly628Val
|
|
XM_005255984.4:c.1862G>T
|
XP_005256041.1:p.Gly621Val
|
|
XM_017023282.1:c.770G>T
|
XP_016878771.1:p.Gly257Val
|
|
XM_017023283.1:c.461G>T
|
XP_016878772.1:p.Gly154Val
|
|
XM_017023284.1:c.461G>T
|
XP_016878773.1:p.Gly154Val
|
|
XR_001751913.1:n.1898G>T
|
|
|
NM_000293.3:c.1883G>T
MANE Select
|
NP_000284.1:p.Gly628Val
|
|
NM_001031835.3:c.1862G>T
|
NP_001027005.1:p.Gly621Val
|
|