ENST00000442544.7:c.*275A>G
MANE Select
|
ENSP00000389140.2:n.*275A>G
|
|
ENST00000412726.5:c.4550A>G
|
ENSP00000397322.2:n.4550A>G
|
|
ENST00000442544.6:c.*275A>G
|
ENSP00000389140.2:n.*275A>G
|
|
NM_005215.3:c.*275A>G
|
NP_005206.2:n.*275A>G
|
|
XM_011525844.1:c.*275A>G
|
XP_011524146.1:n.*275A>G
|
|
XM_011525844.2:c.*275A>G
|
XP_011524146.1:n.*275A>G
|
|
XM_017025568.1:c.*275A>G
|
XP_016881057.1:n.*275A>G
|
|
XM_017025569.1:c.*275A>G
|
XP_016881058.1:n.*275A>G
|
|
XM_017025570.1:c.*275A>G
|
XP_016881059.1:n.*275A>G
|
|
NM_005215.4:c.*275A>G
MANE Select
|
NP_005206.2:n.*275A>G
|
|