ENST00000379644.9:c.1444A>G
MANE Select
|
ENSP00000368965.4:p.Met482Val
|
|
ENST00000379644.8:c.1444A>G
|
ENSP00000368965.4:p.Met482Val
|
|
ENST00000520678.1:n.377A>G
|
|
|
ENST00000521576.1:c.595A>G
|
ENSP00000429029.1:p.Met199Val
|
|
ENST00000524016.5:c.548A>G
|
|
|
NM_152419.2:c.1444A>G
|
NP_689632.2:p.Met482Val
|
|
XM_005273409.1:c.1444A>G
|
XP_005273466.1:p.Met482Val
|
|
XM_005273410.1:c.1444A>G
|
XP_005273467.1:p.Met482Val
|
|
XM_005273411.1:c.1252A>G
|
XP_005273468.1:p.Met418Val
|
|
XM_005273412.2:c.1444A>G
|
XP_005273469.1:p.Met482Val
|
|
NM_001363227.1:c.1444A>G
|
NP_001350156.1:p.Met482Val
|
|
NM_001363228.1:c.1252A>G
|
NP_001350157.1:p.Met418Val
|
|
NM_001363229.1:c.580A>G
|
NP_001350158.1:p.Met194Val
|
|
XM_005273412.4:c.1444A>G
|
XP_005273469.1:p.Met482Val
|
|
NM_152419.3:c.1444A>G
MANE Select
|
NP_689632.2:p.Met482Val
|
|
NM_001363227.2:c.1444A>G
|
NP_001350156.1:p.Met482Val
|
|
NM_001363228.2:c.1252A>G
|
NP_001350157.1:p.Met418Val
|
|
NM_001363229.2:c.580A>G
|
NP_001350158.1:p.Met194Val
|
|