ENST00000328300.11:c.4217G>C
MANE Select
|
ENSP00000331902.7:p.Gly1406Ala
|
|
ENST00000361603.7:c.4199G>C
|
ENSP00000354505.2:p.Gly1400Ala
|
|
ENST00000510690.2:n.711G>C
|
|
|
ENST00000328300.10:c.4217G>C
|
ENSP00000331902.6:p.Gly1406Ala
|
|
ENST00000361603.6:c.4199G>C
|
ENSP00000354505.2:p.Gly1400Ala
|
|
ENST00000489230.1:n.620G>C
|
|
|
ENST00000515658.1:c.13G>C
|
|
|
NM_000495.4:c.4199G>C
|
NP_000486.1:p.Gly1400Ala
|
|
NM_033380.2:c.4217G>C
|
NP_203699.1:p.Gly1406Ala
|
|
XM_005262070.2:c.4208G>C
|
XP_005262127.1:p.Gly1403Ala
|
|
XM_006724616.2:c.4217G>C
|
XP_006724679.1:p.Gly1406Ala
|
|
XM_011530849.1:c.3893G>C
|
XP_011529151.1:p.Gly1298Ala
|
|
XM_011530851.1:c.1790G>C
|
XP_011529153.1:p.Gly597Ala
|
|
XM_011530849.2:c.4232G>C
|
XP_011529151.2:p.Gly1411Ala
|
|
XM_017029259.2:c.4223G>C
|
XP_016884748.1:p.Gly1408Ala
|
|
XM_017029260.1:c.4214G>C
|
XP_016884749.1:p.Gly1405Ala
|
|
XM_017029263.2:c.2552G>C
|
XP_016884752.1:p.Gly851Ala
|
|
NM_000495.5:c.4199G>C
|
NP_000486.1:p.Gly1400Ala
|
|
NM_033380.3:c.4217G>C
MANE Select
|
NP_203699.1:p.Gly1406Ala
|
|