ENST00000288840.10:c.1099T>G
MANE Select
|
ENSP00000288840.5:p.Cys367Gly
|
|
ENST00000288840.9:c.1099T>G
|
ENSP00000288840.5:p.Cys367Gly
|
|
ENST00000557916.5:c.1231T>G
|
ENSP00000452955.1:n.1231T>G
|
|
ENST00000559931.5:c.403T>G
|
ENSP00000453446.1:n.403T>G
|
|
NM_005585.4:c.1099T>G
|
NP_005576.3:p.Cys367Gly
|
|
NR_027654.1:n.2154T>G
|
|
|
XM_011521561.1:c.316T>G
|
XP_011519863.1:p.Cys106Gly
|
|
XR_931825.1:n.2498T>G
|
|
|
XM_011521561.2:c.316T>G
|
XP_011519863.1:p.Cys106Gly
|
|
NM_005585.5:c.1099T>G
MANE Select
|
NP_005576.3:p.Cys367Gly
|
|
NR_027654.2:n.2254T>G
|
|
|