ENST00000369846.9:c.-192+4450T>G
MANE Select
|
ENSP00000358861.4:n.-192+4450T>G
|
|
ENST00000369846.8:c.-192+4450T>G
|
ENSP00000358861.4:n.-192+4450T>G
|
|
ENST00000392959.5:c.-298+4401T>G
|
ENSP00000376686.1:n.-298+4401T>G
|
|
ENST00000467898.3:c.-192+4528T>G
|
ENSP00000474463.1:n.-192+4528T>G
|
|
NM_001122769.2:c.-192+4450T>G
|
NP_001116241.1:n.-192+4450T>G
|
|
NM_181714.3:c.-298+4401T>G
|
NP_859065.2:n.-298+4401T>G
|
|
XM_005248665.3:c.-192+4401T>G
|
XP_005248722.1:n.-192+4401T>G
|
|
XM_011535504.1:c.-298+4450T>G
|
XP_011533806.1:n.-298+4450T>G
|
|
XM_005248665.4:c.-192+4401T>G
|
XP_005248722.1:n.-192+4401T>G
|
|
NM_001122769.3:c.-192+4450T>G
MANE Select
|
NP_001116241.1:n.-192+4450T>G
|
|
NM_181714.4:c.-298+4401T>G
|
NP_859065.2:n.-298+4401T>G
|
|