ENST00000399503.4:c.3053C>T
MANE Select
|
ENSP00000382423.3:p.Ser1018Phe
|
|
ENST00000399503.3:c.3053C>T
|
ENSP00000382423.3:p.Ser1018Phe
|
|
NM_005921.1:c.3053C>T
|
NP_005912.1:p.Ser1018Phe
|
|
XM_005248519.3:c.2675C>T
|
XP_005248576.2:p.Ser892Phe
|
|
XM_011543406.1:c.2798C>T
|
XP_011541708.1:p.Ser933Phe
|
|
XM_011543407.1:c.2774C>T
|
XP_011541709.1:p.Ser925Phe
|
|
XM_011543408.1:c.3053C>T
|
XP_011541710.1:p.Ser1018Phe
|
|
XM_017009484.1:c.2642C>T
|
XP_016864973.1:p.Ser881Phe
|
|
XM_017009485.1:c.2564C>T
|
XP_016864974.1:p.Ser855Phe
|
|
XR_001742068.2:n.3084C>T
|
|
|
NM_005921.2:c.3053C>T
MANE Select
|
NP_005912.1:p.Ser1018Phe
|
|