ENST00000324071.10:c.1088T>G
MANE Select
|
ENSP00000324648.2:p.Leu363Arg
|
|
ENST00000598834.2:c.1112T>G
|
|
|
ENST00000324071.8:c.1088T>G
|
ENSP00000324648.2:p.Leu363Arg
|
|
ENST00000593831.1:c.380T>G
|
ENSP00000470582.1:p.Leu127Arg
|
|
ENST00000597612.1:n.583T>G
|
|
|
NM_000767.4:c.1088T>G
|
NP_000758.1:p.Leu363Arg
|
|
XM_005258569.3:c.1088T>G
|
XP_005258626.1:p.Leu363Arg
|
|
XM_006723050.2:c.1088T>G
|
XP_006723113.1:p.Leu363Arg
|
|
XM_011526546.1:c.1088T>G
|
XP_011524848.1:p.Leu363Arg
|
|
XM_011526547.1:c.1088T>G
|
XP_011524849.1:p.Leu363Arg
|
|
XM_011526548.1:c.608T>G
|
XP_011524850.1:p.Leu203Arg
|
|
XM_011526549.1:c.497T>G
|
XP_011524851.1:p.Leu166Arg
|
|
XM_011526550.1:c.488T>G
|
XP_011524852.1:p.Leu163Arg
|
|
NM_000767.5:c.1088T>G
MANE Select
|
NP_000758.1:p.Leu363Arg
|
|