ENST00000398603.6:c.337-212A>G
|
ENSP00000381604.1:n.337-212A>G
|
|
ENST00000398606.10:c.410A>G
MANE Select
|
ENSP00000381607.3:p.Asn137Ser
|
|
ENST00000646888.1:c.*126A>G
|
ENSP00000494477.1:n.*126A>G
|
|
ENST00000398603.5:c.337-212A>G
|
ENSP00000381604.1:n.337-212A>G
|
|
ENST00000398606.7:c.410A>G
|
ENSP00000381607.3:p.Asn137Ser
|
|
ENST00000467591.1:n.521A>G
|
|
|
ENST00000494593.1:n.1205A>G
|
|
|
ENST00000495996.1:c.74A>G
|
ENSP00000484686.1:p.Asn25Ser
|
|
ENST00000498765.5:c.473A>G
|
|
|
NM_000852.3:c.410A>G , LRG_723t1:c.410A>G
|
NP_000843.1:p.Asn137Ser
|
|
NM_000852.4:c.410A>G
MANE Select
|
NP_000843.1:p.Asn137Ser
|
|