ENST00000255078.8:c.901G>T
MANE Select
|
ENSP00000255078.4:p.Asp301Tyr
|
|
ENST00000539224.2:c.1030G>T
|
|
|
ENST00000674955.1:c.901G>T
|
ENSP00000502463.1:p.Asp301Tyr
|
|
ENST00000675118.1:c.248G>T
|
|
|
ENST00000675119.1:c.190G>T
|
ENSP00000501861.1:p.Asp64Tyr
|
|
ENST00000675305.1:c.190G>T
|
ENSP00000502365.1:p.Asp64Tyr
|
|
ENST00000675464.1:c.190G>T
|
ENSP00000502650.1:p.Asp64Tyr
|
|
ENST00000675615.1:c.901G>T
|
ENSP00000502413.1:p.Asp301Tyr
|
|
ENST00000675683.1:c.288G>T
|
|
|
ENST00000676173.1:n.945G>T
|
|
|
ENST00000676228.1:c.*224G>T
|
ENSP00000502375.1:n.*224G>T
|
|
ENST00000676239.1:n.215G>T
|
|
|
ENST00000255078.7:c.901G>T
|
ENSP00000255078.3:p.Asp301Tyr
|
|
NM_002180.2:c.901G>T , LRG_250t1:c.901G>T
|
NP_002171.2:p.Asp301Tyr
|
|
XM_005273974.2:c.-111G>T
|
XP_005274031.1:n.-111G>T
|
|
XM_005273976.1:c.901G>T
|
XP_005274033.1:p.Asp301Tyr
|
|
XR_247198.1:n.1003G>T
|
|
|
XR_949903.1:n.1003G>T
|
|
|
XM_005273976.2:c.901G>T
|
XP_005274033.1:p.Asp301Tyr
|
|
XM_017017669.2:c.-111G>T
|
XP_016873158.1:n.-111G>T
|
|
XM_017017670.2:c.-111G>T
|
XP_016873159.1:n.-111G>T
|
|
XM_017017671.2:c.901G>T
|
XP_016873160.1:p.Asp301Tyr
|
|
XR_949903.3:n.999G>T
|
|
|
NM_002180.3:c.901G>T
MANE Select
|
NP_002171.2:p.Asp301Tyr
|
|