ENST00000181839.10:c.2090G>T
MANE Select
|
ENSP00000181839.4:p.Trp697Leu
|
|
ENST00000340829.10:c.2090G>T
|
ENSP00000340557.5:p.Trp697Leu
|
|
ENST00000484589.2:c.642G>T
|
|
|
ENST00000642213.1:n.572G>T
|
|
|
ENST00000643859.1:c.981G>T
|
|
|
ENST00000643915.1:c.404G>T
|
ENSP00000496187.1:p.Trp135Leu
|
|
ENST00000645470.1:c.20G>T
|
ENSP00000495036.1:p.Trp7Leu
|
|
ENST00000646039.1:c.1430G>T
|
ENSP00000494168.1:p.Trp477Leu
|
|
ENST00000646437.1:c.724G>T
|
|
|
ENST00000647453.1:n.1159G>T
|
|
|
ENST00000647518.1:n.3927G>T
|
|
|
ENST00000181839.8:c.2090G>T
|
ENSP00000181839.4:p.Trp697Leu
|
|
ENST00000340829.9:c.2090G>T
|
ENSP00000340557.5:p.Trp697Leu
|
|
ENST00000484589.1:n.642G>T
|
|
|
ENST00000611390.1:c.248G>T
|
ENSP00000484610.1:p.Trp83Leu
|
|
ENST00000613626.4:c.248G>T
|
ENSP00000480835.1:p.Trp83Leu
|
|
NM_003718.4:c.2090G>T
|
NP_003709.3:p.Trp697Leu
|
|
NM_031267.3:c.2090G>T
|
NP_112557.2:p.Trp697Leu
|
|
XM_011515597.1:c.2090G>T
|
XP_011513899.1:p.Trp697Leu
|
|
XM_011515598.1:c.2090G>T
|
XP_011513900.1:p.Trp697Leu
|
|
XM_011515597.3:c.2090G>T
|
XP_011513899.1:p.Trp697Leu
|
|
XM_017012750.2:c.2090G>T
|
XP_016868239.1:p.Trp697Leu
|
|
XM_017012751.2:c.2090G>T
|
XP_016868240.1:p.Trp697Leu
|
|
NM_003718.5:c.2090G>T
MANE Select
|
NP_003709.3:p.Trp697Leu
|
|