NM_001244710.2:c.1879G>A
MANE Select
|
NP_001231639.1:p.Val627Met
|
ENST00000357308.9:c.1879G>A
MANE Select
|
ENSP00000349860.4:p.Val627Met
|
NM_001244710.1:c.1879G>A , LRG_787t1:c.1879G>A
|
NP_001231639.1:p.Val627Met
|
NM_002056.3:c.1825G>A
|
NP_002047.2:p.Val609Met
|
NM_002056.4:c.1825G>A
|
NP_002047.2:p.Val609Met
|
ENST00000357308.8:c.1879G>A
|
ENSP00000349860.4:p.Val627Met
|
ENST00000361060.5:c.1825G>A
|
ENSP00000354347.4:p.Val609Met
|
ENST00000674438.1:c.1609G>A
|
ENSP00000501469.1:p.Val537Met
|
ENST00000674507.1:c.1671+1012G>A
|
ENSP00000501332.1:n.1671+1012G>A
|
XM_017003801.1:c.1954G>A
|
XP_016859290.1:p.Val652Met
|
XM_017003802.2:c.1900G>A
|
XP_016859291.1:p.Val634Met
|