ENST00000498907.3:c.386C>G
MANE Select
|
ENSP00000427514.1:p.Pro129Arg
|
|
ENST00000498907.2:c.386C>G
|
ENSP00000427514.1:p.Pro129Arg
|
|
NM_001285829.1:c.29C>G
|
NP_001272758.1:p.Pro10Arg
|
|
NM_001287424.1:c.491C>G
|
NP_001274353.1:p.Pro164Arg
|
|
NM_001287435.1:c.344C>G
|
NP_001274364.1:p.Pro115Arg
|
|
NM_004364.4:c.386C>G
|
NP_004355.2:p.Pro129Arg
|
|
NM_001287424.2:c.491C>G
|
NP_001274353.1:p.Pro164Arg
|
|
NM_004364.5:c.386C>G
MANE Select
|
NP_004355.2:p.Pro129Arg
|
|
NM_001285829.2:c.29C>G
|
NP_001272758.1:p.Pro10Arg
|
|
NM_001287435.2:c.344C>G
|
NP_001274364.1:p.Pro115Arg
|
|