ENST00000474370.2:n.2385G>A
|
|
|
ENST00000492391.2:n.1536G>A
|
|
|
ENST00000682645.1:n.3483G>A
|
|
|
ENST00000683432.1:c.*587G>A
|
ENSP00000508174.1:n.*587G>A
|
|
ENST00000684207.1:c.412G>A
|
ENSP00000506942.1:p.Glu138Lys
|
|
ENST00000297157.8:c.412G>A
MANE Select
|
ENSP00000297157.3:p.Glu138Lys
|
|
ENST00000297157.7:c.412G>A
|
ENSP00000297157.3:p.Glu138Lys
|
|
ENST00000448915.1:c.310G>A
|
ENSP00000411577.1:p.Glu104Lys
|
|
NM_203288.1:c.412G>A
|
NP_976033.1:p.Glu138Lys
|
|
XM_011515468.1:c.310G>A
|
XP_011513770.1:p.Glu104Lys
|
|
XM_011515468.3:c.310G>A
|
XP_011513770.1:p.Glu104Lys
|
|
NM_203288.2:c.412G>A
MANE Select
|
NP_976033.1:p.Glu138Lys
|
|