ENST00000619706.5:c.1730A=
MANE Select
|
ENSP00000480469.1:p.Glu577=
|
|
ENST00000316316.10:c.1730A=
|
ENSP00000314505.5:p.Glu577=
|
|
ENST00000458674.2:c.207-1065A=
|
|
|
ENST00000619706.4:c.1730A=
|
ENSP00000480469.1:p.Glu577=
|
|
NM_017696.2:c.1730A=
|
NP_060166.2:p.Glu577=
|
|
NM_001378356.1:c.1730A=
|
NP_001365285.1:p.Glu577=
|
|
NM_001378357.1:c.1730A=
|
NP_001365286.1:p.Glu577=
|
|
NM_001378359.1:c.1730A=
|
NP_001365288.1:p.Glu577=
|
|
NM_001378360.1:c.1730A=
|
NP_001365289.1:p.Glu577=
|
|
NM_001378364.1:c.1529-1065A=
|
NP_001365293.1:n.1529-1065A=
|
|
NM_001378366.1:c.1604A=
|
NP_001365295.1:p.Glu535=
|
|
NM_001378367.1:c.1532A=
|
NP_001365296.1:p.Glu511=
|
|
NM_017696.3:c.1730A=
MANE Select
|
NP_060166.2:p.Glu577=
|
|
NR_165493.1:n.1839A=
|
|
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