ENST00000430374.6:c.-183G>T
|
ENSP00000405077.2:n.-183G>T
|
|
ENST00000444508.6:c.-314G>T
|
ENSP00000398969.2:n.-314G>T
|
|
ENST00000697898.1:n.134G>T
|
|
|
ENST00000697899.1:c.-228G>T
|
ENSP00000513470.1:n.-228G>T
|
|
ENST00000697900.1:n.49G>T
|
|
|
ENST00000697901.1:c.-228G>T
|
ENSP00000513471.1:n.-228G>T
|
|
ENST00000697902.1:n.5G>T
|
|
|
ENST00000697903.1:c.-228G>T
|
ENSP00000513472.1:n.-228G>T
|
|
ENST00000357276.9:c.-228G>T
MANE Select
|
ENSP00000349823.4:n.-228G>T
|
|
ENST00000357276.8:c.-228G>T
|
ENSP00000349823.4:n.-228G>T
|
|
ENST00000430374.5:c.-183G>T
|
ENSP00000405077.1:n.-183G>T
|
|
ENST00000444508.5:c.-314G>T
|
ENSP00000398969.1:n.-314G>T
|
|
NM_014140.3:c.-228G>T , LRG_108t1:c.-228G>T
|
NP_054859.2:n.-228G>T
|
|
XM_005246631.2:c.-183G>T
|
XP_005246688.1:n.-183G>T
|
|
XM_005246632.1:c.-314G>T
|
XP_005246689.1:n.-314G>T
|
|
XM_006712557.1:c.-228G>T
|
XP_006712620.1:n.-228G>T
|
|
NM_014140.4:c.-228G>T
MANE Select
|
NP_054859.2:n.-228G>T
|
|