ENST00000216714.8:c.578G>A
MANE Select
|
ENSP00000216714.3:p.Arg193His
|
|
ENST00000216714.7:c.578G>A
|
ENSP00000216714.3:p.Arg193His
|
|
ENST00000398030.8:c.578G>A
|
ENSP00000381111.4:p.Arg193His
|
|
ENST00000438886.1:c.358G>A
|
|
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ENST00000553555.5:n.998G>A
|
|
|
ENST00000553681.5:c.578G>A
|
ENSP00000451327.1:p.Arg193His
|
|
ENST00000554813.5:n.644G>A
|
|
|
ENST00000555414.5:c.578G>A
|
ENSP00000451979.1:p.Arg193His
|
|
ENST00000555839.5:c.491G>A
|
ENSP00000452460.1:p.Arg164His
|
|
ENST00000557054.1:c.34G>A
|
ENSP00000452212.2:p.Ala12Thr
|
|
ENST00000557159.5:n.1194G>A
|
|
|
ENST00000557365.1:n.658G>A
|
|
|
NM_001244249.1:c.578G>A
|
NP_001231178.1:p.Arg193His
|
|
NM_001641.3:c.578G>A
|
NP_001632.2:p.Arg193His
|
|
NM_080648.2:c.578G>A
|
NP_542379.1:p.Arg193His
|
|
NM_080649.2:c.578G>A
|
NP_542380.1:p.Arg193His
|
|
XM_005267581.3:c.578G>A
|
XP_005267638.1:p.Arg193His
|
|
XM_005267582.3:c.527G>A
|
XP_005267639.1:p.Arg176His
|
|
NM_001641.4:c.578G>A
MANE Select
|
NP_001632.2:p.Arg193His
|
|
NM_001244249.2:c.578G>A
|
NP_001231178.1:p.Arg193His
|
|
NM_080648.3:c.578G>A
|
NP_542379.1:p.Arg193His
|
|
NM_080649.3:c.578G>A
|
NP_542380.1:p.Arg193His
|
|