ENST00000324071.10:c.1074A>G
MANE Select
|
ENSP00000324648.2:p.Arg358=
|
|
ENST00000598834.2:c.1098A>G
|
|
|
ENST00000324071.8:c.1074A>G
|
ENSP00000324648.2:p.Arg358=
|
|
ENST00000593831.1:c.366A>G
|
ENSP00000470582.1:p.Arg122=
|
|
ENST00000597612.1:n.569A>G
|
|
|
NM_000767.4:c.1074A>G
|
NP_000758.1:p.Arg358=
|
|
XM_005258569.3:c.1074A>G
|
XP_005258626.1:p.Arg358=
|
|
XM_006723050.2:c.1074A>G
|
XP_006723113.1:p.Arg358=
|
|
XM_011526546.1:c.1074A>G
|
XP_011524848.1:p.Arg358=
|
|
XM_011526547.1:c.1074A>G
|
XP_011524849.1:p.Arg358=
|
|
XM_011526548.1:c.594A>G
|
XP_011524850.1:p.Arg198=
|
|
XM_011526549.1:c.483A>G
|
XP_011524851.1:p.Arg161=
|
|
XM_011526550.1:c.474A>G
|
XP_011524852.1:p.Arg158=
|
|
NM_000767.5:c.1074A>G
MANE Select
|
NP_000758.1:p.Arg358=
|
|