ENST00000322776.11:c.700G=
MANE Select
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ENSP00000322450.6:p.Gly234=
|
|
ENST00000647561.1:c.700G=
|
ENSP00000497587.1:p.Gly234=
|
|
ENST00000322776.10:c.700G=
|
ENSP00000322450.6:p.Gly234=
|
|
ENST00000415352.6:c.679G=
|
ENSP00000395368.2:p.Gly227=
|
|
ENST00000526169.1:n.442G=
|
|
|
ENST00000526770.5:n.559G=
|
|
|
ENST00000529927.5:c.673G=
|
ENSP00000436766.1:p.Gly225=
|
|
ENST00000532244.5:c.397G=
|
ENSP00000435202.1:p.Gly133=
|
|
ENST00000532303.5:c.397G=
|
ENSP00000432015.1:p.Gly133=
|
|
ENST00000533919.5:c.178G=
|
ENSP00000435199.1:p.Gly60=
|
|
NM_001166102.1:c.673G=
|
NP_001159574.1:p.Gly225=
|
|
NM_007103.3:c.700G=
|
NP_009034.2:p.Gly234=
|
|
NM_001166102.2:c.673G=
|
NP_001159574.1:p.Gly225=
|
|
NM_007103.4:c.700G=
MANE Select
|
NP_009034.2:p.Gly234=
|
|