ENST00000398603.6:c.337-270G>C
|
ENSP00000381604.1:n.337-270G>C
|
|
ENST00000398606.10:c.352G>C
MANE Select
|
ENSP00000381607.3:p.Asp118His
|
|
ENST00000646888.1:c.*68G>C
|
ENSP00000494477.1:n.*68G>C
|
|
ENST00000398603.5:c.337-270G>C
|
ENSP00000381604.1:n.337-270G>C
|
|
ENST00000398606.7:c.352G>C
|
ENSP00000381607.3:p.Asp118His
|
|
ENST00000467591.1:n.463G>C
|
|
|
ENST00000494593.1:n.1147G>C
|
|
|
ENST00000495996.1:c.16G>C
|
ENSP00000484686.1:p.Asp6His
|
|
ENST00000498765.5:c.415G>C
|
|
|
NM_000852.3:c.352G>C , LRG_723t1:c.352G>C
|
NP_000843.1:p.Asp118His
|
|
NM_000852.4:c.352G>C
MANE Select
|
NP_000843.1:p.Asp118His
|
|