ENST00000324071.10:c.335G>C
MANE Select
|
ENSP00000324648.2:p.Gly112Ala
|
|
ENST00000598834.2:c.237G>C
|
|
|
ENST00000324071.8:c.335G>C
|
ENSP00000324648.2:p.Gly112Ala
|
|
ENST00000593831.1:c.107G>C
|
ENSP00000470582.1:p.Gly36Ala
|
|
ENST00000598834.1:n.237G>C
|
|
|
NM_000767.4:c.335G>C
|
NP_000758.1:p.Gly112Ala
|
|
XM_005258569.3:c.335G>C
|
XP_005258626.1:p.Gly112Ala
|
|
XM_006723050.2:c.335G>C
|
XP_006723113.1:p.Gly112Ala
|
|
XM_011526546.1:c.335G>C
|
XP_011524848.1:p.Gly112Ala
|
|
XM_011526547.1:c.335G>C
|
XP_011524849.1:p.Gly112Ala
|
|
XM_011526548.1:c.335G>C
|
XP_011524850.1:p.Gly112Ala
|
|
XM_011526550.1:c.215G>C
|
XP_011524852.1:p.Gly72Ala
|
|
NM_000767.5:c.335G>C
MANE Select
|
NP_000758.1:p.Gly112Ala
|
|