ENST00000700472.1:c.*528A>C
|
ENSP00000515005.1:n.*528A>C
|
|
ENST00000264033.6:c.1076A>C
MANE Select
|
ENSP00000264033.3:p.Asp359Ala
|
|
ENST00000637974.1:c.1070A>C
|
ENSP00000490763.1:p.Asp357Ala
|
|
ENST00000264033.5:c.1076A>C
|
ENSP00000264033.3:p.Asp359Ala
|
|
ENST00000634586.1:c.1076A>C
|
ENSP00000489218.1:p.Asp359Ala
|
|
ENST00000634840.1:c.1076A>C
|
ENSP00000489324.1:p.Asp359Ala
|
|
NM_005188.3:c.1076A>C , LRG_608t1:c.1076A>C
|
NP_005179.2:p.Asp359Ala
|
|
XM_011543057.1:c.1076A>C
|
XP_011541359.1:p.Asp359Ala
|
|
NM_005188.4:c.1076A>C
MANE Select
|
NP_005179.2:p.Asp359Ala
|
|