ENST00000255078.8:c.2294A>T
MANE Select
|
ENSP00000255078.4:p.His765Leu
|
|
ENST00000674675.1:c.538A>T
|
|
|
ENST00000674878.1:c.538A>T
|
|
|
ENST00000674955.1:c.*1011A>T
|
ENSP00000502463.1:n.*1011A>T
|
|
ENST00000675118.1:c.1782A>T
|
|
|
ENST00000675389.1:n.569A>T
|
|
|
ENST00000675615.1:c.2294A>T
|
ENSP00000502413.1:p.His765Leu
|
|
ENST00000675648.1:n.1669A>T
|
|
|
ENST00000675916.1:c.538A>T
|
|
|
ENST00000676173.1:n.3039A>T
|
|
|
ENST00000676182.1:c.725A>T
|
|
|
ENST00000676228.1:c.*1617A>T
|
ENSP00000502375.1:n.*1617A>T
|
|
ENST00000255078.7:c.2294A>T
|
ENSP00000255078.3:p.His765Leu
|
|
ENST00000539064.5:n.2053A>T
|
|
|
ENST00000543739.5:n.1287A>T
|
|
|
NM_002180.2:c.2294A>T , LRG_250t1:c.2294A>T
|
NP_002171.2:p.His765Leu
|
|
XM_005273974.2:c.1283A>T
|
XP_005274031.1:p.His428Leu
|
|
XM_005273975.2:c.1166A>T
|
XP_005274032.1:p.His389Leu
|
|
XM_011544994.1:c.1061A>T
|
XP_011543296.1:p.His354Leu
|
|
XR_949903.1:n.2396A>T
|
|
|
XM_005273975.3:c.1166A>T
|
XP_005274032.1:p.His389Leu
|
|
XM_017017669.2:c.1283A>T
|
XP_016873158.1:p.His428Leu
|
|
XM_017017670.2:c.1283A>T
|
XP_016873159.1:p.His428Leu
|
|
XR_949903.3:n.2392A>T
|
|
|
NM_002180.3:c.2294A>T
MANE Select
|
NP_002171.2:p.His765Leu
|
|