ENST00000378756.8:c.51G>T
MANE Select
|
ENSP00000368031.3:p.Gly17=
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ENST00000672388.1:n.155G>T
|
|
|
ENST00000378755.9:c.51G>T
|
ENSP00000368030.5:p.Gly17=
|
|
ENST00000378756.7:c.51G>T
|
ENSP00000368031.3:p.Gly17=
|
|
NM_001170535.1:c.51G>T
|
NP_001164006.1:p.Gly17=
|
|
NM_018188.3:c.51G>T
|
NP_060658.3:p.Gly17=
|
|
NM_001170535.2:c.51G>T
|
NP_001164006.1:p.Gly17=
|
|
NM_018188.4:c.51G>T
|
NP_060658.3:p.Gly17=
|
|
XM_024448098.1:c.51G>T
|
XP_024303866.1:p.Gly17=
|
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XR_001737282.1:n.177G>T
|
|
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XR_002956997.1:n.177G>T
|
|
|
NM_001170535.3:c.51G>T
MANE Select
|
NP_001164006.1:p.Gly17=
|
|
NM_018188.5:c.51G>T
|
NP_060658.3:p.Gly17=
|
|