ENST00000224721.12:c.8469G>T
MANE Select
|
ENSP00000224721.9:p.Leu2823=
|
|
ENST00000642965.1:c.2402G>T
|
ENSP00000495222.1:n.2402G>T
|
|
ENST00000647092.1:c.2066G>T
|
ENSP00000495176.1:n.2066G>T
|
|
ENST00000224721.10:c.8484G>T
|
ENSP00000224721.8:p.Leu2828=
|
|
ENST00000398788.4:c.1749G>T
|
ENSP00000381768.3:p.Leu583=
|
|
ENST00000475158.1:n.2005G>T
|
|
|
ENST00000619887.4:c.1749G>T
|
ENSP00000478374.1:p.Leu583=
|
|
ENST00000622827.4:c.8469G>T
|
ENSP00000483211.1:p.Leu2823=
|
|
NM_001171933.1:c.1749G>T
|
NP_001165404.1:p.Leu583=
|
|
NM_001171934.1:c.1749G>T
|
NP_001165405.1:p.Leu583=
|
|
NM_022124.5:c.8469G>T
|
NP_071407.4:p.Leu2823=
|
|
XM_006717940.2:c.8664G>T
|
XP_006718003.1:p.Leu2888=
|
|
XM_006717942.2:c.8598G>T
|
XP_006718005.1:p.Leu2866=
|
|
XM_011540039.1:c.8661G>T
|
XP_011538341.1:p.Leu2887=
|
|
XM_011540040.1:c.8658G>T
|
XP_011538342.1:p.Leu2886=
|
|
XM_011540041.1:c.8604G>T
|
XP_011538343.1:p.Leu2868=
|
|
XM_011540042.1:c.8574G>T
|
XP_011538344.1:p.Leu2858=
|
|
XM_011540043.1:c.8664G>T
|
XP_011538345.1:p.Leu2888=
|
|
XM_011540044.1:c.8529G>T
|
XP_011538346.1:p.Leu2843=
|
|
XM_011540045.1:c.8664G>T
|
XP_011538347.1:p.Leu2888=
|
|
XM_011540046.1:c.8124G>T
|
XP_011538348.1:p.Leu2708=
|
|
XM_011540047.1:c.7482G>T
|
XP_011538349.1:p.Leu2494=
|
|
XM_011540052.1:c.4992G>T
|
XP_011538354.1:p.Leu1664=
|
|
NM_022124.6:c.8469G>T
MANE Select
|
NP_071407.4:p.Leu2823=
|
|