ENST00000617875.6:c.442G>T
MANE Select
|
ENSP00000482313.2:p.Val148Phe
|
|
ENST00000524998.1:c.228-264G>T
|
|
|
ENST00000534538.1:c.309-16G>T
|
|
|
ENST00000617875.4:c.442G>T
|
ENSP00000482313.1:p.Val148Phe
|
|
ENST00000621189.4:c.-630G>T
|
ENSP00000483145.1:n.-630G>T
|
|
NM_004260.3:c.442G>T
|
NP_004251.3:p.Val148Phe
|
|
XM_011517380.1:c.442G>T
|
XP_011515682.1:p.Val148Phe
|
|
XM_011517381.1:c.442G>T
|
XP_011515683.1:p.Val148Phe
|
|
XM_011517382.1:c.442G>T
|
XP_011515684.1:p.Val148Phe
|
|
XM_011517383.1:c.442G>T
|
XP_011515685.1:p.Val148Phe
|
|
XM_011517384.1:c.442G>T
|
XP_011515686.1:p.Val148Phe
|
|
XR_928366.1:n.483G>T
|
|
|
XR_928367.1:n.483G>T
|
|
|
XR_928368.1:n.485G>T
|
|
|
XM_011517384.3:c.442G>T
|
XP_011515686.1:p.Val148Phe
|
|
XM_017013991.2:c.442G>T
|
XP_016869480.1:p.Val148Phe
|
|
XM_017013992.2:c.442G>T
|
XP_016869481.1:p.Val148Phe
|
|
XM_017013993.2:c.442G>T
|
XP_016869482.1:p.Val148Phe
|
|
XM_017013994.2:c.442G>T
|
XP_016869483.1:p.Val148Phe
|
|
XM_017013995.2:c.442G>T
|
XP_016869484.1:p.Val148Phe
|
|
XM_017013996.2:c.442G>T
|
XP_016869485.1:p.Val148Phe
|
|
XM_017013997.2:c.442G>T
|
XP_016869486.1:p.Val148Phe
|
|
XM_017013998.1:c.442G>T
|
XP_016869487.1:p.Val148Phe
|
|
XM_017013999.2:c.442G>T
|
XP_016869488.1:p.Val148Phe
|
|
XM_017014001.2:c.-692G>T
|
XP_016869490.1:n.-692G>T
|
|
XR_001745626.2:n.479G>T
|
|
|
XR_001745627.2:n.479G>T
|
|
|
XR_001745628.2:n.479G>T
|
|
|
XR_001745629.2:n.479G>T
|
|
|
XR_001745630.2:n.479G>T
|
|
|
NM_004260.4:c.442G>T
MANE Select
|
NP_004251.4:p.Val148Phe
|
|