|
ENST00000046640.9:c.712A>G
MANE Select
|
ENSP00000046640.4:p.Ile238Val
|
|
|
ENST00000381870.8:c.712A>G
|
ENSP00000371294.3:p.Ile238Val
|
|
|
ENST00000488623.6:c.-42A>G
|
ENSP00000501016.1:n.-42A>G
|
|
|
ENST00000574776.6:c.271A>G
|
ENSP00000461118.2:p.Ile91Val
|
|
|
ENST00000673669.1:c.271A>G
|
ENSP00000501123.1:p.Ile91Val
|
|
|
ENST00000673965.1:c.712A>G
|
ENSP00000500995.1:p.Ile238Val
|
|
|
ENST00000046640.7:c.712A>G
|
ENSP00000046640.3:p.Ile238Val
|
|
|
ENST00000381870.7:c.712A>G
|
ENSP00000371294.3:p.Ile238Val
|
|
|
NM_001031681.2:c.712A>G
|
NP_001026851.2:p.Ile238Val
|
|
|
NM_004937.2:c.712A>G
|
NP_004928.2:p.Ile238Val
|
|
|
XM_005256485.1:c.712A>G
|
XP_005256542.1:p.Ile238Val
|
|
|
XM_006721463.1:c.712A>G
|
XP_006721526.1:p.Ile238Val
|
|
|
XM_006721464.1:c.271A>G
|
XP_006721527.1:p.Ile91Val
|
|
|
XM_011523691.1:c.712A>G
|
XP_011521993.1:p.Ile238Val
|
|
|
XM_011523692.1:c.271A>G
|
XP_011521994.1:p.Ile91Val
|
|
|
XR_934003.1:n.1305A>G
|
|
|
|
XM_005256485.3:c.712A>G
|
XP_005256542.1:p.Ile238Val
|
|
|
XM_006721463.3:c.712A>G
|
XP_006721526.1:p.Ile238Val
|
|
|
XM_006721464.2:c.271A>G
|
XP_006721527.1:p.Ile91Val
|
|
|
XM_011523691.2:c.712A>G
|
XP_011521993.1:p.Ile238Val
|
|
|
XM_011523692.2:c.271A>G
|
XP_011521994.1:p.Ile91Val
|
|
|
XM_017024254.1:c.271A>G
|
XP_016879743.1:p.Ile91Val
|
|
|
XM_017024255.1:c.271A>G
|
XP_016879744.1:p.Ile91Val
|
|
|
XM_017024256.1:c.271A>G
|
XP_016879745.1:p.Ile91Val
|
|
|
XM_017024257.1:c.271A>G
|
XP_016879746.1:p.Ile91Val
|
|
|
XM_017024258.1:c.271A>G
|
XP_016879747.1:p.Ile91Val
|
|
|
NM_001374492.1:c.712A>G
|
NP_001361421.1:p.Ile238Val
|
|
|
NM_001374493.1:c.271A>G
|
NP_001361422.1:p.Ile91Val
|
|
|
NM_001374494.1:c.271A>G
|
NP_001361423.1:p.Ile91Val
|
|
|
NM_001374495.1:c.271A>G
|
NP_001361424.1:p.Ile91Val
|
|
|
NM_001374496.1:c.271A>G
|
NP_001361425.1:p.Ile91Val
|
|
|
NM_004937.3:c.712A>G
MANE Select
|
NP_004928.2:p.Ile238Val
|
|
|
NM_001031681.3:c.712A>G
|
NP_001026851.2:p.Ile238Val
|
|
