ENST00000257904.11:c.626G>C
MANE Select
|
ENSP00000257904.5:p.Arg209Pro
|
|
ENST00000257904.10:c.626G>C
|
ENSP00000257904.5:p.Arg209Pro
|
|
ENST00000312990.10:c.274G>C
|
ENSP00000316889.6:p.Val92Leu
|
|
ENST00000546489.5:c.404G>C
|
ENSP00000447779.1:p.Arg135Pro
|
|
ENST00000547281.5:c.404G>C
|
ENSP00000447274.1:p.Arg135Pro
|
|
ENST00000549606.5:c.-157-1158G>C
|
ENSP00000447005.1:n.-157-1158G>C
|
|
ENST00000550419.5:c.523-99G>C
|
ENSP00000448098.1:n.523-99G>C
|
|
ENST00000551888.5:n.452G>C
|
|
|
ENST00000553237.5:c.*265G>C
|
ENSP00000448885.1:n.*265G>C
|
|
NM_000075.3:c.626G>C
|
NP_000066.1:p.Arg209Pro
|
|
NM_000075.4:c.626G>C
MANE Select
|
NP_000066.1:p.Arg209Pro
|
|