ENST00000435030.6:c.710A>T
MANE Select
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ENSP00000393379.1:p.Glu237Val
|
|
ENST00000464066.6:n.575A>T
|
|
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ENST00000676875.1:n.1101A>T
|
|
|
ENST00000677280.1:c.710A>T
|
ENSP00000503955.1:p.Glu237Val
|
|
ENST00000677747.1:c.710A>T
|
ENSP00000504145.1:p.Glu237Val
|
|
ENST00000677843.1:c.710A>T
|
ENSP00000504362.1:p.Glu237Val
|
|
ENST00000677891.1:c.710A>T
|
ENSP00000503013.1:p.Glu237Val
|
|
ENST00000678056.1:c.710A>T
|
ENSP00000503535.1:p.Glu237Val
|
|
ENST00000678133.1:n.3562A>T
|
|
|
ENST00000678160.1:c.710A>T
|
ENSP00000503636.1:p.Glu237Val
|
|
ENST00000678291.1:n.1101A>T
|
|
|
ENST00000435030.5:c.710A>T
|
ENSP00000393379.1:p.Glu237Val
|
|
NM_004522.2:c.710A>T
|
NP_004513.1:p.Glu237Val
|
|
XR_922926.1:n.1096A>T
|
|
|
XM_017004062.1:c.710A>T
|
XP_016859551.1:p.Glu237Val
|
|
NM_004522.3:c.710A>T
MANE Select
|
NP_004513.1:p.Glu237Val
|
|