ENST00000239440.9:c.2806C>T
MANE Select
|
ENSP00000239440.4:p.Arg936Trp
|
|
ENST00000239440.8:c.2806C>T
|
ENSP00000239440.4:p.Arg936Trp
|
|
ENST00000508305.5:c.2507-461C>T
|
ENSP00000421826.1:n.2507-461C>T
|
|
ENST00000512390.1:n.555C>T
|
|
|
ENST00000513878.5:c.1792C>T
|
ENSP00000421468.1:p.Arg598Trp
|
|
ENST00000626478.2:c.2507-461C>T
|
ENSP00000486980.1:n.2507-461C>T
|
|
NM_022481.5:c.2806C>T
|
NP_071926.4:p.Arg936Trp
|
|
XM_005268497.1:c.2806C>T
|
XP_005268554.1:p.Arg936Trp
|
|
XM_005268498.1:c.2806C>T
|
XP_005268555.1:p.Arg936Trp
|
|
XM_005268499.1:c.2572C>T
|
XP_005268556.1:p.Arg858Trp
|
|
XM_006714792.1:c.2801-461C>T
|
XP_006714855.1:n.2801-461C>T
|
|
XM_011537677.1:c.2221C>T
|
XP_011535979.1:p.Arg741Trp
|
|
XR_944326.1:n.2733C>T
|
|
|
XR_944328.1:n.2728-461C>T
|
|
|
XR_944329.1:n.2945C>T
|
|
|
XM_005268497.2:c.2806C>T
|
XP_005268554.1:p.Arg936Trp
|
|
XM_005268498.2:c.2806C>T
|
XP_005268555.1:p.Arg936Trp
|
|
XM_006714792.2:c.2801-461C>T
|
XP_006714855.1:n.2801-461C>T
|
|
XM_011537677.2:c.2221C>T
|
XP_011535979.1:p.Arg741Trp
|
|
XR_944329.3:n.2974C>T
|
|
|
NM_022481.6:c.2806C>T
MANE Select
|
NP_071926.4:p.Arg936Trp
|
|