ENST00000255078.8:c.2374G>T
MANE Select
|
ENSP00000255078.4:p.Ala792Ser
|
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ENST00000674675.1:c.587+31G>T
|
|
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ENST00000674878.1:c.548-69G>T
|
|
|
ENST00000674955.1:c.*1091G>T
|
ENSP00000502463.1:n.*1091G>T
|
|
ENST00000675118.1:c.1862G>T
|
|
|
ENST00000675389.1:n.649G>T
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|
|
ENST00000675615.1:c.2374G>T
|
ENSP00000502413.1:p.Ala792Ser
|
|
ENST00000675648.1:n.1749G>T
|
|
|
ENST00000675916.1:c.618G>T
|
|
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ENST00000676173.1:n.3119G>T
|
|
|
ENST00000676182.1:c.805G>T
|
|
|
ENST00000676228.1:c.*1697G>T
|
ENSP00000502375.1:n.*1697G>T
|
|
ENST00000255078.7:c.2374G>T
|
ENSP00000255078.3:p.Ala792Ser
|
|
ENST00000539064.5:n.2133G>T
|
|
|
ENST00000543739.5:n.1367G>T
|
|
|
NM_002180.2:c.2374G>T , LRG_250t1:c.2374G>T
|
NP_002171.2:p.Ala792Ser
|
|
XM_005273974.2:c.1363G>T
|
XP_005274031.1:p.Ala455Ser
|
|
XM_005273975.2:c.1246G>T
|
XP_005274032.1:p.Ala416Ser
|
|
XM_011544994.1:c.1141G>T
|
XP_011543296.1:p.Ala381Ser
|
|
XR_949903.1:n.2476G>T
|
|
|
XM_005273975.3:c.1246G>T
|
XP_005274032.1:p.Ala416Ser
|
|
XM_017017669.2:c.1363G>T
|
XP_016873158.1:p.Ala455Ser
|
|
XM_017017670.2:c.1363G>T
|
XP_016873159.1:p.Ala455Ser
|
|
XR_949903.3:n.2472G>T
|
|
|
NM_002180.3:c.2374G>T
MANE Select
|
NP_002171.2:p.Ala792Ser
|
|