ENST00000442544.7:c.1735G>T
MANE Select
|
ENSP00000389140.2:p.Asp579Tyr
|
|
ENST00000304775.12:c.1536G>T
|
|
|
ENST00000412726.5:c.1666G>T
|
ENSP00000397322.2:p.Asp556Tyr
|
|
ENST00000442544.6:c.1735G>T
|
ENSP00000389140.2:p.Asp579Tyr
|
|
ENST00000581580.5:c.700G>T
|
ENSP00000464582.1:p.Asp234Tyr
|
|
NM_005215.3:c.1735G>T
|
NP_005206.2:p.Asp579Tyr
|
|
XM_011525843.1:c.1735G>T
|
XP_011524145.1:p.Asp579Tyr
|
|
XM_011525844.1:c.700G>T
|
XP_011524146.1:p.Asp234Tyr
|
|
XM_011525845.1:c.1735G>T
|
XP_011524147.1:p.Asp579Tyr
|
|
XM_011525846.1:c.1735G>T
|
XP_011524148.1:p.Asp579Tyr
|
|
XM_011525844.2:c.700G>T
|
XP_011524146.1:p.Asp234Tyr
|
|
XM_017025568.1:c.1735G>T
|
XP_016881057.1:p.Asp579Tyr
|
|
XM_017025569.1:c.1735G>T
|
XP_016881058.1:p.Asp579Tyr
|
|
XM_017025570.1:c.700G>T
|
XP_016881059.1:p.Asp234Tyr
|
|
NM_005215.4:c.1735G>T
MANE Select
|
NP_005206.2:p.Asp579Tyr
|
|