ENST00000255078.8:c.877G>T
MANE Select
|
ENSP00000255078.4:p.Val293Phe
|
|
ENST00000539224.2:c.1006G>T
|
|
|
ENST00000674955.1:c.877G>T
|
ENSP00000502463.1:p.Val293Phe
|
|
ENST00000675118.1:c.224G>T
|
|
|
ENST00000675119.1:c.166G>T
|
ENSP00000501861.1:p.Val56Phe
|
|
ENST00000675305.1:c.166G>T
|
ENSP00000502365.1:p.Val56Phe
|
|
ENST00000675464.1:c.166G>T
|
ENSP00000502650.1:p.Val56Phe
|
|
ENST00000675615.1:c.877G>T
|
ENSP00000502413.1:p.Val293Phe
|
|
ENST00000675683.1:c.264G>T
|
|
|
ENST00000676173.1:n.921G>T
|
|
|
ENST00000676228.1:c.*200G>T
|
ENSP00000502375.1:n.*200G>T
|
|
ENST00000676239.1:n.191G>T
|
|
|
ENST00000255078.7:c.877G>T
|
ENSP00000255078.3:p.Val293Phe
|
|
NM_002180.2:c.877G>T , LRG_250t1:c.877G>T
|
NP_002171.2:p.Val293Phe
|
|
XM_005273974.2:c.-135G>T
|
XP_005274031.1:n.-135G>T
|
|
XM_005273976.1:c.877G>T
|
XP_005274033.1:p.Val293Phe
|
|
XR_247198.1:n.979G>T
|
|
|
XR_949903.1:n.979G>T
|
|
|
XM_005273976.2:c.877G>T
|
XP_005274033.1:p.Val293Phe
|
|
XM_017017669.2:c.-135G>T
|
XP_016873158.1:n.-135G>T
|
|
XM_017017670.2:c.-135G>T
|
XP_016873159.1:n.-135G>T
|
|
XM_017017671.2:c.877G>T
|
XP_016873160.1:p.Val293Phe
|
|
XR_949903.3:n.975G>T
|
|
|
NM_002180.3:c.877G>T
MANE Select
|
NP_002171.2:p.Val293Phe
|
|