ENST00000340855.11:c.1120G>C
MANE Select
|
ENSP00000339801.6:p.Gly374Arg
|
|
ENST00000651111.1:c.487G>C
|
ENSP00000498395.1:p.Gly163Arg
|
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ENST00000340855.10:c.1120G>C
|
ENSP00000339801.6:p.Gly374Arg
|
|
ENST00000422081.6:c.487G>C
|
ENSP00000477056.1:p.Gly163Arg
|
|
ENST00000441880.1:n.227G>C
|
|
|
NM_000202.6:c.1120G>C
|
NP_000193.1:p.Gly374Arg
|
|
NM_001166550.2:c.850G>C
|
NP_001160022.1:p.Gly284Arg
|
|
NM_000202.7:c.1120G>C
|
NP_000193.1:p.Gly374Arg
|
|
NM_001166550.3:c.850G>C
|
NP_001160022.1:p.Gly284Arg
|
|
NM_000202.8:c.1120G>C
MANE Select
|
NP_000193.1:p.Gly374Arg
|
|
NM_001166550.4:c.850G>C
|
NP_001160022.1:p.Gly284Arg
|
|