ENST00000553591.2:c.692A>C
|
ENSP00000452421.2:p.Tyr231Ser
|
|
ENST00000556293.6:n.2998A>C
|
|
|
ENST00000556754.2:n.3941A>C
|
|
|
ENST00000557229.6:n.1004A>C
|
|
|
ENST00000697613.1:c.575A>C
|
ENSP00000513359.1:p.Tyr192Ser
|
|
ENST00000697614.1:c.338A>C
|
ENSP00000513360.1:p.Tyr113Ser
|
|
ENST00000697615.1:n.1403A>C
|
|
|
ENST00000361505.10:c.575A>C
MANE Select
|
ENSP00000354532.6:p.Tyr192Ser
|
|
ENST00000361505.9:c.575A>C
|
ENSP00000354532.5:p.Tyr192Ser
|
|
ENST00000554056.5:n.883A>C
|
|
|
ENST00000556754.1:n.1792A>C
|
|
|
NM_000270.3:c.575A>C , LRG_91t1:c.575A>C
|
NP_000261.2:p.Tyr192Ser
|
|
NM_000270.4:c.575A>C
MANE Select
|
NP_000261.2:p.Tyr192Ser
|
|