ENST00000553591.2:c.602T>A
|
ENSP00000452421.2:p.Met201Lys
|
|
ENST00000556293.6:n.2908T>A
|
|
|
ENST00000556754.2:n.3851T>A
|
|
|
ENST00000557229.6:n.914T>A
|
|
|
ENST00000697613.1:c.485T>A
|
ENSP00000513359.1:p.Met162Lys
|
|
ENST00000697614.1:c.248T>A
|
ENSP00000513360.1:p.Met83Lys
|
|
ENST00000697615.1:n.1313T>A
|
|
|
ENST00000361505.10:c.485T>A
MANE Select
|
ENSP00000354532.6:p.Met162Lys
|
|
ENST00000361505.9:c.485T>A
|
ENSP00000354532.5:p.Met162Lys
|
|
ENST00000553591.1:c.602T>A
|
ENSP00000452421.1:p.Met201Lys
|
|
ENST00000554056.5:n.793T>A
|
|
|
ENST00000556754.1:n.1702T>A
|
|
|
ENST00000557229.5:n.914T>A
|
|
|
NM_000270.3:c.485T>A , LRG_91t1:c.485T>A
|
NP_000261.2:p.Met162Lys
|
|
NM_000270.4:c.485T>A
MANE Select
|
NP_000261.2:p.Met162Lys
|
|