ENST00000288774.8:c.576C>T
|
ENSP00000288774.3:p.Ala192=
|
|
ENST00000447513.7:c.576C>T
MANE Select
|
ENSP00000407922.2:p.Ala192=
|
|
ENST00000650293.1:c.530C>T
|
|
|
ENST00000288774.7:c.576C>T
|
ENSP00000288774.3:p.Ala192=
|
|
ENST00000447513.6:c.576C>T
|
ENSP00000407922.2:p.Ala192=
|
|
ENST00000507596.5:c.576C>T
|
ENSP00000424291.1:p.Ala192=
|
|
ENST00000510434.1:c.576C>T
|
ENSP00000423051.1:p.Ala192=
|
|
NM_002617.3:c.576C>T
|
NP_002608.1:p.Ala192=
|
|
NM_153818.1:c.576C>T
|
NP_722540.1:p.Ala192=
|
|
XM_011541573.1:c.576C>T
|
XP_011539875.1:p.Ala192=
|
|
XM_011541574.1:c.144C>T
|
XP_011539876.1:p.Ala48=
|
|
XM_011541575.1:c.144C>T
|
XP_011539877.1:p.Ala48=
|
|
XM_011541576.1:c.576C>T
|
XP_011539878.1:p.Ala192=
|
|
XR_946666.1:n.696C>T
|
|
|
XM_011541576.2:c.576C>T
|
XP_011539878.1:p.Ala192=
|
|
XR_946666.2:n.645C>T
|
|
|
NM_001374425.1:c.576C>T
|
NP_001361354.1:p.Ala192=
|
|
NM_001374426.1:c.144C>T
|
NP_001361355.1:p.Ala48=
|
|
NM_001374427.1:c.144C>T
|
NP_001361356.1:p.Ala48=
|
|
NM_002617.4:c.576C>T
MANE Select
|
NP_002608.1:p.Ala192=
|
|
NM_153818.2:c.576C>T
|
NP_722540.1:p.Ala192=
|
|
NR_164636.1:n.695C>T
|
|
|