ENST00000374736.8:c.4963G>T
MANE Select
|
ENSP00000363868.3:p.Val1655Phe
|
|
ENST00000678995.1:c.4969G>T
|
ENSP00000504612.1:p.Val1657Phe
|
|
ENST00000374736.7:c.4963G>T
|
ENSP00000363868.3:p.Val1655Phe
|
|
NM_005502.3:c.4963G>T
|
NP_005493.2:p.Val1655Phe
|
|
XM_005251773.1:c.4969G>T
|
XP_005251830.1:p.Val1657Phe
|
|
XM_005251776.1:c.4789G>T
|
XP_005251833.1:p.Val1597Phe
|
|
XM_011518339.1:c.5044G>T
|
XP_011516641.1:p.Val1682Phe
|
|
XM_011518340.1:c.5044G>T
|
XP_011516642.1:p.Val1682Phe
|
|
XM_011518341.1:c.5038G>T
|
XP_011516643.1:p.Val1680Phe
|
|
XM_011518342.1:c.4606G>T
|
XP_011516644.1:p.Val1536Phe
|
|
XM_011518343.1:c.5044G>T
|
XP_011516645.1:p.Val1682Phe
|
|
XM_005251773.3:c.4969G>T
|
XP_005251830.1:p.Val1657Phe
|
|
XM_005251776.3:c.4789G>T
|
XP_005251833.1:p.Val1597Phe
|
|
XM_011518339.3:c.5044G>T
|
XP_011516641.1:p.Val1682Phe
|
|
XM_011518340.3:c.5044G>T
|
XP_011516642.1:p.Val1682Phe
|
|
XM_011518341.3:c.5038G>T
|
XP_011516643.1:p.Val1680Phe
|
|
XM_011518342.3:c.4606G>T
|
XP_011516644.1:p.Val1536Phe
|
|
XM_017014378.2:c.5044G>T
|
XP_016869867.1:p.Val1682Phe
|
|
XM_017014379.2:c.5044G>T
|
XP_016869868.1:p.Val1682Phe
|
|
XM_017014380.2:c.5044G>T
|
XP_016869869.1:p.Val1682Phe
|
|
XM_017014381.2:c.5044G>T
|
XP_016869870.1:p.Val1682Phe
|
|
XM_017014382.2:c.4906G>T
|
XP_016869871.1:p.Val1636Phe
|
|
XR_001746223.1:n.5357G>T
|
|
|
NM_005502.4:c.4963G>T
MANE Select
|
NP_005493.2:p.Val1655Phe
|
|