ENST00000541682.7:c.367C>G
MANE Select
|
ENSP00000446205.2:p.Leu123Val
|
|
ENST00000317814.8:c.352C>G
|
ENSP00000314774.4:p.Leu118Val
|
|
ENST00000541682.6:c.367C>G
|
ENSP00000446205.2:p.Leu123Val
|
|
ENST00000577735.1:c.343C>G
|
ENSP00000462491.1:p.Leu115Val
|
|
NM_001165967.1:c.367C>G
|
NP_001159439.1:p.Leu123Val
|
|
NM_032580.3:c.352C>G
|
NP_115969.2:p.Leu118Val
|
|
XM_011524038.1:c.472C>G
|
XP_011522340.1:p.Leu158Val
|
|
XM_011524039.1:c.463C>G
|
XP_011522341.1:p.Leu155Val
|
|
XM_011524040.1:c.463C>G
|
XP_011522342.1:p.Leu155Val
|
|
XM_011524041.1:c.454C>G
|
XP_011522343.1:p.Leu152Val
|
|
XM_011524042.1:c.325C>G
|
XP_011522344.1:p.Leu109Val
|
|
XR_934203.1:n.69+2083G>C
|
|
|
XM_017025232.1:c.472C>G
|
XP_016880721.1:p.Leu158Val
|
|
XM_024451007.1:c.472C>G
|
XP_024306775.1:p.Leu158Val
|
|
NM_001165967.2:c.367C>G
MANE Select
|
NP_001159439.1:p.Leu123Val
|
|
NM_032580.4:c.352C>G
|
NP_115969.2:p.Leu118Val
|
|