ENST00000388996.10:c.991C>G
MANE Select
|
ENSP00000373648.3:p.Leu331Val
|
|
ENST00000521134.6:c.631C>G
|
ENSP00000429799.1:p.Leu211Val
|
|
ENST00000638588.1:c.664C>G
|
ENSP00000491940.1:p.Leu222Val
|
|
ENST00000639358.1:c.641C>G
|
|
|
ENST00000639496.1:c.664C>G
|
ENSP00000491165.1:p.Leu222Val
|
|
ENST00000388996.8:c.991C>G
|
ENSP00000373648.3:p.Leu331Val
|
|
ENST00000519445.5:c.991C>G
|
ENSP00000428790.1:p.Leu331Val
|
|
ENST00000519589.1:n.769C>G
|
|
|
ENST00000521134.5:c.631C>G
|
ENSP00000429799.1:p.Leu211Val
|
|
ENST00000621976.1:c.628C>G
|
ENSP00000482510.1:p.Leu210Val
|
|
NM_001204824.1:c.631C>G
|
NP_001191753.1:p.Leu211Val
|
|
NM_004519.3:c.991C>G
|
NP_004510.1:p.Leu331Val
|
|
XM_005250914.2:c.-166C>G
|
XP_005250971.1:n.-166C>G
|
|
XM_006716555.2:c.283C>G
|
XP_006716618.1:p.Leu95Val
|
|
XM_011517026.1:c.631C>G
|
XP_011515328.1:p.Leu211Val
|
|
XM_005250914.3:c.-166C>G
|
XP_005250971.1:n.-166C>G
|
|
XM_006716555.3:c.283C>G
|
XP_006716618.1:p.Leu95Val
|
|
XM_011517026.2:c.631C>G
|
XP_011515328.1:p.Leu211Val
|
|
XM_017013400.1:c.769C>G
|
XP_016868889.1:p.Leu257Val
|
|
NM_004519.4:c.991C>G
MANE Select
|
NP_004510.1:p.Leu331Val
|
|
NM_001204824.2:c.631C>G
|
NP_001191753.1:p.Leu211Val
|
|