ENST00000280097.5:c.524G>C
MANE Select
|
ENSP00000280097.3:p.Gly175Ala
|
|
ENST00000280097.4:c.524G>C
|
ENSP00000280097.3:p.Gly175Ala
|
|
ENST00000410115.5:c.524G>C
|
ENSP00000386940.1:p.Gly175Ala
|
|
ENST00000485653.1:n.456G>C
|
|
|
NM_006895.2:c.524G>C
|
NP_008826.1:p.Gly175Ala
|
|
XM_011511063.1:c.422G>C
|
XP_011509365.1:p.Gly141Ala
|
|
XM_011511064.1:c.146G>C
|
XP_011509366.1:p.Gly49Ala
|
|
XM_011511064.2:c.146G>C
|
XP_011509366.1:p.Gly49Ala
|
|
XM_017003948.1:c.422G>C
|
XP_016859437.1:p.Gly141Ala
|
|
XR_001739719.1:n.232-5979C>G
|
|
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XR_002959286.1:n.911G>C
|
|
|
NM_006895.3:c.524G>C
MANE Select
|
NP_008826.1:p.Gly175Ala
|
|