|
ENST00000360774.6:c.1945G>T
MANE Select
|
ENSP00000354006.1:p.Ala649Ser
|
|
|
ENST00000360774.5:c.1945G>T
|
ENSP00000354006.1:p.Ala649Ser
|
|
|
ENST00000361255.7:c.1930G>T
|
ENSP00000354962.3:p.Ala644Ser
|
|
|
ENST00000449912.6:c.1930G>T
|
ENSP00000396672.2:p.Ala644Ser
|
|
|
NM_001177310.1:c.1930G>T
|
NP_001170781.1:p.Ala644Ser
|
|
|
NM_001177311.1:c.1930G>T
|
NP_001170782.1:p.Ala644Ser
|
|
|
NM_017662.4:c.1945G>T
|
NP_060132.3:p.Ala649Ser
|
|
|
XM_011518244.1:c.1945G>T
|
XP_011516546.1:p.Ala649Ser
|
|
|
XM_011518245.1:c.1852G>T
|
XP_011516547.1:p.Ala618Ser
|
|
|
XM_011518246.1:c.1945G>T
|
XP_011516548.1:p.Ala649Ser
|
|
|
XM_011518247.1:c.1945G>T
|
XP_011516549.1:p.Ala649Ser
|
|
|
XM_011518248.1:c.1804G>T
|
XP_011516550.1:p.Ala602Ser
|
|
|
XM_011518249.1:c.1711G>T
|
XP_011516551.1:p.Ala571Ser
|
|
|
XM_011518250.1:c.1945G>T
|
XP_011516552.1:p.Ala649Ser
|
|
|
XM_011518251.1:c.1216G>T
|
XP_011516553.1:p.Ala406Ser
|
|
|
XM_011518252.1:c.1945G>T
|
XP_011516554.1:p.Ala649Ser
|
|
|
XM_011518253.1:c.-119G>T
|
XP_011516555.1:n.-119G>T
|
|
|
XM_011518254.1:c.1945G>T
|
XP_011516556.1:p.Ala649Ser
|
|
|
XM_011518255.1:c.1945G>T
|
XP_011516557.1:p.Ala649Ser
|
|
|
XR_929716.1:n.2183G>T
|
|
|
|
XR_929717.1:n.2183G>T
|
|
|
|
XR_929718.1:n.2183G>T
|
|
|
|
XM_011518251.2:c.1216G>T
|
XP_011516553.1:p.Ala406Ser
|
|
|
XM_011518252.2:c.1945G>T
|
XP_011516554.1:p.Ala649Ser
|
|
|
XM_011518255.2:c.1945G>T
|
XP_011516557.1:p.Ala649Ser
|
|
|
XM_017014287.1:c.1711G>T
|
XP_016869776.1:p.Ala571Ser
|
|
|
XM_017014288.1:c.1711G>T
|
XP_016869777.1:p.Ala571Ser
|
|
|
XM_017014289.1:c.1945G>T
|
XP_016869778.1:p.Ala649Ser
|
|
|
XR_001746185.1:n.2183G>T
|
|
|
|
XR_929717.2:n.2183G>T
|
|
|
|
NM_017662.5:c.1945G>T
MANE Select
|
NP_060132.3:p.Ala649Ser
|
|
|
NM_001177310.2:c.1930G>T
|
NP_001170781.1:p.Ala644Ser
|
|
|
NM_001177311.2:c.1930G>T
|
NP_001170782.1:p.Ala644Ser
|
|
