ENST00000265512.12:c.-41T>G
MANE Select
|
ENSP00000265512.7:n.-41T>G
|
|
ENST00000265512.11:c.-41T>G
|
ENSP00000265512.7:n.-41T>G
|
|
ENST00000504125.1:c.-41T>G
|
ENSP00000427525.1:n.-41T>G
|
|
ENST00000504581.1:n.170-1483T>G
|
|
|
ENST00000504894.1:c.-102T>G
|
ENSP00000427261.1:n.-102T>G
|
|
ENST00000505590.5:c.-124T>G
|
ENSP00000425416.1:n.-124T>G
|
|
ENST00000506705.5:c.-124T>G
|
ENSP00000426667.1:n.-124T>G
|
|
ENST00000508393.5:c.-132T>G
|
ENSP00000424630.1:n.-132T>G
|
|
ENST00000629236.2:c.-41T>G
|
ENSP00000486450.1:n.-41T>G
|
|
NM_000670.3:c.-41T>G
|
NP_000661.2:n.-41T>G
|
|
NM_000670.4:c.-41T>G
|
NP_000661.2:n.-41T>G
|
|
NM_001306171.1:c.-132T>G
|
NP_001293100.1:n.-132T>G
|
|
NM_001306172.1:c.-124T>G
|
NP_001293101.1:n.-124T>G
|
|
NR_037884.1:n.680-10282A>C
|
|
|
XR_938685.1:n.48T>G
|
|
|
XR_938686.1:n.31T>G
|
|
|
XR_938687.1:n.52T>G
|
|
|
NM_000670.5:c.-41T>G
MANE Select
|
NP_000661.2:n.-41T>G
|
|
NM_001306171.2:c.-132T>G
|
NP_001293100.1:n.-132T>G
|
|
NM_001306172.2:c.-124T>G
|
NP_001293101.1:n.-124T>G
|
|