ENST00000398019.7:c.*504A>T
MANE Select
|
ENSP00000381101.2:n.*504A>T
|
|
ENST00000336429.6:c.*504A>T
|
ENSP00000337212.2:n.*504A>T
|
|
ENST00000398019.6:c.*504A>T
|
ENSP00000381101.2:n.*504A>T
|
|
ENST00000540675.5:c.*504A>T
|
ENSP00000444572.1:n.*504A>T
|
|
ENST00000546027.5:c.*504A>T
|
ENSP00000444861.1:n.*504A>T
|
|
NM_001040147.2:c.*504A>T
|
NP_001035237.1:n.*504A>T
|
|
NM_001261830.1:c.*504A>T
|
NP_001248759.1:n.*504A>T
|
|
NM_001261831.1:c.*504A>T
|
NP_001248760.1:n.*504A>T
|
|
NM_003784.3:c.*504A>T
|
NP_003775.1:n.*504A>T
|
|
XM_006722562.1:c.*504A>T
|
XP_006722625.1:n.*504A>T
|
|
XM_011526236.1:c.*504A>T
|
XP_011524538.1:n.*504A>T
|
|
XM_024451278.1:c.*504A>T
|
XP_024307046.1:n.*504A>T
|
|
NM_003784.4:c.*504A>T
MANE Select
|
NP_003775.1:n.*504A>T
|
|
NM_001040147.3:c.*504A>T
|
NP_001035237.1:n.*504A>T
|
|
NM_001261830.2:c.*504A>T
|
NP_001248759.1:n.*504A>T
|
|
NM_001261831.2:c.*504A>T
|
NP_001248760.1:n.*504A>T
|
|