ENST00000273183.8:c.184C>A
MANE Select
|
ENSP00000273183.3:p.Gln62Lys
|
|
ENST00000273183.7:c.184C>A
|
ENSP00000273183.3:p.Gln62Lys
|
|
ENST00000427486.5:c.112-39556C>A
|
ENSP00000397521.1:n.112-39556C>A
|
|
ENST00000434649.1:c.151C>A
|
ENSP00000398403.1:p.Gln51Lys
|
|
ENST00000457375.6:c.184C>A
|
ENSP00000393713.2:p.Gln62Lys
|
|
ENST00000476388.5:n.379C>A
|
|
|
ENST00000486143.1:n.143C>A
|
|
|
NM_001292049.1:c.184C>A
|
NP_001278978.1:p.Gln62Lys
|
|
NM_003149.2:c.184C>A
|
NP_003140.1:p.Gln62Lys
|
|
XM_011534036.1:c.196C>A
|
XP_011532338.1:p.Gln66Lys
|
|
XM_011534037.1:c.151C>A
|
XP_011532339.1:p.Gln51Lys
|
|
XM_011534038.1:c.-21C>A
|
XP_011532340.1:n.-21C>A
|
|
XR_940496.1:n.382C>A
|
|
|
XM_011534037.3:c.151C>A
|
XP_011532339.1:p.Gln51Lys
|
|
XM_011534038.2:c.-21C>A
|
XP_011532340.1:n.-21C>A
|
|
XM_017007083.1:c.-21C>A
|
XP_016862572.1:n.-21C>A
|
|
XM_024453722.1:c.196C>A
|
XP_024309490.1:p.Gln66Lys
|
|
XM_024453723.1:c.196C>A
|
XP_024309491.1:p.Gln66Lys
|
|
XR_940496.2:n.366C>A
|
|
|
NM_001292049.2:c.184C>A
|
NP_001278978.1:p.Gln62Lys
|
|
NM_003149.3:c.184C>A
MANE Select
|
NP_003140.1:p.Gln62Lys
|
|