ENST00000255078.8:c.2160G>T
MANE Select
|
ENSP00000255078.4:p.Val720=
|
|
ENST00000674675.1:c.404G>T
|
|
|
ENST00000674878.1:c.404G>T
|
|
|
ENST00000674955.1:c.*877G>T
|
ENSP00000502463.1:n.*877G>T
|
|
ENST00000675118.1:c.1648G>T
|
|
|
ENST00000675389.1:n.435G>T
|
|
|
ENST00000675615.1:c.2160G>T
|
ENSP00000502413.1:p.Val720=
|
|
ENST00000675648.1:n.1535G>T
|
|
|
ENST00000675916.1:c.404G>T
|
|
|
ENST00000676173.1:n.2905G>T
|
|
|
ENST00000676182.1:c.591G>T
|
|
|
ENST00000676228.1:c.*1483G>T
|
ENSP00000502375.1:n.*1483G>T
|
|
ENST00000255078.7:c.2160G>T
|
ENSP00000255078.3:p.Val720=
|
|
ENST00000539064.5:n.1919G>T
|
|
|
ENST00000543739.5:n.1153G>T
|
|
|
NM_002180.2:c.2160G>T , LRG_250t1:c.2160G>T
|
NP_002171.2:p.Val720=
|
|
XM_005273974.2:c.1149G>T
|
XP_005274031.1:p.Val383=
|
|
XM_005273975.2:c.1032G>T
|
XP_005274032.1:p.Val344=
|
|
XM_011544994.1:c.927G>T
|
XP_011543296.1:p.Val309=
|
|
XR_949903.1:n.2262G>T
|
|
|
XM_005273975.3:c.1032G>T
|
XP_005274032.1:p.Val344=
|
|
XM_017017669.2:c.1149G>T
|
XP_016873158.1:p.Val383=
|
|
XM_017017670.2:c.1149G>T
|
XP_016873159.1:p.Val383=
|
|
XR_949903.3:n.2258G>T
|
|
|
NM_002180.3:c.2160G>T
MANE Select
|
NP_002171.2:p.Val720=
|
|