ENST00000224721.12:c.8310C>G
MANE Select
|
ENSP00000224721.9:p.Ala2770=
|
|
ENST00000642965.1:c.2243C>G
|
ENSP00000495222.1:n.2243C>G
|
|
ENST00000647092.1:c.1907C>G
|
ENSP00000495176.1:n.1907C>G
|
|
ENST00000224721.10:c.8325C>G
|
ENSP00000224721.8:p.Ala2775=
|
|
ENST00000398788.4:c.1590C>G
|
ENSP00000381768.3:p.Ala530=
|
|
ENST00000475158.1:n.1846C>G
|
|
|
ENST00000619887.4:c.1590C>G
|
ENSP00000478374.1:p.Ala530=
|
|
ENST00000622827.4:c.8310C>G
|
ENSP00000483211.1:p.Ala2770=
|
|
NM_001171933.1:c.1590C>G
|
NP_001165404.1:p.Ala530=
|
|
NM_001171934.1:c.1590C>G
|
NP_001165405.1:p.Ala530=
|
|
NM_022124.5:c.8310C>G
|
NP_071407.4:p.Ala2770=
|
|
XM_006717940.2:c.8505C>G
|
XP_006718003.1:p.Ala2835=
|
|
XM_006717942.2:c.8439C>G
|
XP_006718005.1:p.Ala2813=
|
|
XM_011540039.1:c.8502C>G
|
XP_011538341.1:p.Ala2834=
|
|
XM_011540040.1:c.8499C>G
|
XP_011538342.1:p.Ala2833=
|
|
XM_011540041.1:c.8445C>G
|
XP_011538343.1:p.Ala2815=
|
|
XM_011540042.1:c.8415C>G
|
XP_011538344.1:p.Ala2805=
|
|
XM_011540043.1:c.8505C>G
|
XP_011538345.1:p.Ala2835=
|
|
XM_011540044.1:c.8370C>G
|
XP_011538346.1:p.Ala2790=
|
|
XM_011540045.1:c.8505C>G
|
XP_011538347.1:p.Ala2835=
|
|
XM_011540046.1:c.7965C>G
|
XP_011538348.1:p.Ala2655=
|
|
XM_011540047.1:c.7323C>G
|
XP_011538349.1:p.Ala2441=
|
|
XM_011540052.1:c.4833C>G
|
XP_011538354.1:p.Ala1611=
|
|
NM_022124.6:c.8310C>G
MANE Select
|
NP_071407.4:p.Ala2770=
|
|