ENST00000406360.2:c.699G>A
MANE Select
|
ENSP00000385824.1:p.Trp233Ter
|
|
ENST00000343882.10:c.699G>A
|
ENSP00000339527.6:p.Trp233Ter
|
|
ENST00000406360.1:c.699G>A
|
ENSP00000385824.1:p.Trp233Ter
|
|
ENST00000540898.1:c.39G>A
|
ENSP00000446316.1:p.Trp13Ter
|
|
NM_001455.3:c.699G>A
|
NP_001446.1:p.Trp233Ter
|
|
NM_201559.2:c.699G>A
|
NP_963853.1:p.Trp233Ter
|
|
XM_005266867.3:c.132G>A
|
XP_005266924.1:p.Trp44Ter
|
|
XM_005266868.2:c.39G>A
|
XP_005266925.1:p.Trp13Ter
|
|
XM_011535626.1:c.198G>A
|
XP_011533928.1:p.Trp66Ter
|
|
XM_011535627.1:c.147G>A
|
XP_011533929.1:p.Trp49Ter
|
|
XM_011535628.1:c.39G>A
|
XP_011533930.1:p.Trp13Ter
|
|
XM_011535629.1:c.39G>A
|
XP_011533931.1:p.Trp13Ter
|
|
XM_005266867.4:c.132G>A
|
XP_005266924.1:p.Trp44Ter
|
|
XM_005266868.3:c.39G>A
|
XP_005266925.1:p.Trp13Ter
|
|
XM_011535626.2:c.198G>A
|
XP_011533928.1:p.Trp66Ter
|
|
XM_011535628.3:c.39G>A
|
XP_011533930.1:p.Trp13Ter
|
|
XM_011535629.2:c.39G>A
|
XP_011533931.1:p.Trp13Ter
|
|
XM_017010585.1:c.132G>A
|
XP_016866074.1:p.Trp44Ter
|
|
XM_017010586.1:c.39G>A
|
XP_016866075.1:p.Trp13Ter
|
|
NM_001455.4:c.699G>A
MANE Select
|
NP_001446.1:p.Trp233Ter
|
|
NM_201559.3:c.699G>A
|
NP_963853.1:p.Trp233Ter
|
|