ENST00000255078.8:c.2062G>T
MANE Select
|
ENSP00000255078.4:p.Ala688Ser
|
|
ENST00000674675.1:c.306G>T
|
|
|
ENST00000674878.1:c.306G>T
|
|
|
ENST00000674955.1:c.*779G>T
|
ENSP00000502463.1:n.*779G>T
|
|
ENST00000675118.1:c.1550G>T
|
|
|
ENST00000675389.1:n.337G>T
|
|
|
ENST00000675615.1:c.2062G>T
|
ENSP00000502413.1:p.Ala688Ser
|
|
ENST00000675648.1:n.1437G>T
|
|
|
ENST00000675916.1:c.306G>T
|
|
|
ENST00000676173.1:n.2807G>T
|
|
|
ENST00000676182.1:c.493G>T
|
|
|
ENST00000676228.1:c.*1385G>T
|
ENSP00000502375.1:n.*1385G>T
|
|
ENST00000255078.7:c.2062G>T
|
ENSP00000255078.3:p.Ala688Ser
|
|
ENST00000539064.5:n.1821G>T
|
|
|
ENST00000543739.5:n.1055G>T
|
|
|
NM_002180.2:c.2062G>T , LRG_250t1:c.2062G>T
|
NP_002171.2:p.Ala688Ser
|
|
XM_005273974.2:c.1051G>T
|
XP_005274031.1:p.Ala351Ser
|
|
XM_005273975.2:c.934G>T
|
XP_005274032.1:p.Ala312Ser
|
|
XM_011544994.1:c.829G>T
|
XP_011543296.1:p.Ala277Ser
|
|
XR_949903.1:n.2164G>T
|
|
|
XM_005273975.3:c.934G>T
|
XP_005274032.1:p.Ala312Ser
|
|
XM_017017669.2:c.1051G>T
|
XP_016873158.1:p.Ala351Ser
|
|
XM_017017670.2:c.1051G>T
|
XP_016873159.1:p.Ala351Ser
|
|
XR_949903.3:n.2160G>T
|
|
|
NM_002180.3:c.2062G>T
MANE Select
|
NP_002171.2:p.Ala688Ser
|
|