ENST00000470094.2:c.*487A>G
|
ENSP00000434898.2:n.*487A>G
|
|
ENST00000528762.2:c.*1331A>G
|
ENSP00000433168.2:n.*1331A>G
|
|
ENST00000530893.7:c.9595A>G
|
ENSP00000499438.2:p.Met3199Val
|
|
ENST00000665585.2:c.*1526A>G
|
ENSP00000499570.2:n.*1526A>G
|
|
ENST00000700202.2:c.9913A>G
|
ENSP00000514856.2:p.Met3305Val
|
|
ENST00000700202.1:c.2380A>G
|
ENSP00000514856.1:p.Met794Val
|
|
ENST00000700203.1:n.2091A>G
|
|
|
ENST00000380152.8:c.9964A>G
MANE Select
|
ENSP00000369497.3:p.Met3322Val
|
|
ENST00000544455.6:c.9964A>G
|
ENSP00000439902.1:p.Met3322Val
|
|
ENST00000614259.2:c.9972A>G
|
ENSP00000506251.1:n.9972A>G
|
|
ENST00000680887.1:c.9964A>G
|
ENSP00000505508.1:p.Met3322Val
|
|
ENST00000380152.7:c.9964A>G
|
ENSP00000369497.3:p.Met3322Val
|
|
ENST00000544455.5:c.9964A>G
|
ENSP00000439902.1:p.Met3322Val
|
|
NM_000059.3:c.9964A>G , LRG_293t1:c.9964A>G
|
NP_000050.2:p.Met3322Val
|
|
XM_011535203.1:c.9964A>G
|
XP_011533505.1:p.Met3322Val
|
|
XM_011535204.1:c.9868A>G
|
XP_011533506.1:p.Met3290Val
|
|
NM_000059.4:c.9964A>G
MANE Select
|
NP_000050.3:p.Met3322Val
|
|