ENST00000298854.7:c.-111T>G
MANE Select
|
ENSP00000298854.2:n.-111T>G
|
|
ENST00000298854.6:c.-111T>G
|
ENSP00000298854.2:n.-111T>G
|
|
ENST00000352508.7:c.-111T>G
|
ENSP00000298853.3:n.-111T>G
|
|
ENST00000524487.5:c.-111T>G
|
ENSP00000435551.2:n.-111T>G
|
|
ENST00000529341.1:c.-111T>G
|
ENSP00000431732.1:n.-111T>G
|
|
NM_005055.4:c.-111T>G
|
NP_005046.2:n.-111T>G
|
|
NM_032645.4:c.-111T>G
|
NP_116034.2:n.-111T>G
|
|
XM_005253042.2:c.-111T>G
|
XP_005253099.1:n.-111T>G
|
|
XM_005253043.2:c.-111T>G
|
XP_005253100.1:n.-111T>G
|
|
XM_011520252.1:c.-111T>G
|
XP_011518554.1:n.-111T>G
|
|
XM_011520253.1:c.-111T>G
|
XP_011518555.1:n.-111T>G
|
|
XM_005253042.3:c.-111T>G
|
XP_005253099.1:n.-111T>G
|
|
XM_005253043.3:c.-111T>G
|
XP_005253100.1:n.-111T>G
|
|
NM_005055.5:c.-111T>G
MANE Select
|
NP_005046.2:n.-111T>G
|
|
NM_032645.5:c.-111T>G
|
NP_116034.2:n.-111T>G
|
|