ENST00000242317.9:c.1825A>G
MANE Select
|
ENSP00000242317.4:p.Ile609Val
|
|
ENST00000242317.8:c.1825A>G
|
ENSP00000242317.4:p.Ile609Val
|
|
ENST00000442556.1:c.329+2552A>G
|
|
|
ENST00000470169.5:c.613A>G
|
|
|
ENST00000485580.1:n.401A>G
|
|
|
ENST00000614641.4:c.1837A>G
|
ENSP00000480538.1:p.Ile613Val
|
|
NM_001281428.1:c.1837A>G
|
NP_001268357.1:p.Ile613Val
|
|
NM_012144.3:c.1825A>G
|
NP_036276.1:p.Ile609Val
|
|
XM_006716758.2:c.1294A>G
|
XP_006716821.1:p.Ile432Val
|
|
XM_011517848.1:c.1579A>G
|
XP_011516150.1:p.Ile527Val
|
|
XM_006716758.3:c.1294A>G
|
XP_006716821.1:p.Ile432Val
|
|
XM_011517848.2:c.1579A>G
|
XP_011516150.1:p.Ile527Val
|
|
XM_017014625.2:c.1567A>G
|
XP_016870114.1:p.Ile523Val
|
|
XR_002956774.1:n.1928A>G
|
|
|
NM_012144.4:c.1825A>G
MANE Select
|
NP_036276.1:p.Ile609Val
|
|
NM_001281428.2:c.1837A>G
|
NP_001268357.1:p.Ile613Val
|
|