ENST00000398603.6:c.337-258G>A
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ENSP00000381604.1:n.337-258G>A
|
|
ENST00000398606.10:c.364G>A
MANE Select
|
ENSP00000381607.3:p.Ala122Thr
|
|
ENST00000646888.1:c.*80G>A
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ENSP00000494477.1:n.*80G>A
|
|
ENST00000398603.5:c.337-258G>A
|
ENSP00000381604.1:n.337-258G>A
|
|
ENST00000398606.7:c.364G>A
|
ENSP00000381607.3:p.Ala122Thr
|
|
ENST00000467591.1:n.475G>A
|
|
|
ENST00000494593.1:n.1159G>A
|
|
|
ENST00000495996.1:c.28G>A
|
ENSP00000484686.1:p.Ala10Thr
|
|
ENST00000498765.5:c.427G>A
|
|
|
NM_000852.3:c.364G>A , LRG_723t1:c.364G>A
|
NP_000843.1:p.Ala122Thr
|
|
NM_000852.4:c.364G>A
MANE Select
|
NP_000843.1:p.Ala122Thr
|
|