ENST00000280097.5:c.338T>C
MANE Select
|
ENSP00000280097.3:p.Phe113Ser
|
|
ENST00000280097.4:c.338T>C
|
ENSP00000280097.3:p.Phe113Ser
|
|
ENST00000410115.5:c.338T>C
|
ENSP00000386940.1:p.Phe113Ser
|
|
ENST00000467390.5:n.350T>C
|
|
|
ENST00000485653.1:n.270T>C
|
|
|
NM_006895.2:c.338T>C
|
NP_008826.1:p.Phe113Ser
|
|
XM_011511063.1:c.236T>C
|
XP_011509365.1:p.Phe79Ser
|
|
XM_011511064.1:c.-41T>C
|
XP_011509366.1:n.-41T>C
|
|
XM_011511064.2:c.-41T>C
|
XP_011509366.1:n.-41T>C
|
|
XM_017003948.1:c.236T>C
|
XP_016859437.1:p.Phe79Ser
|
|
XM_017003949.2:c.338T>C
|
XP_016859438.1:p.Phe113Ser
|
|
XR_001739719.1:n.1039+4886A>G
|
|
|
XR_002959286.1:n.725T>C
|
|
|
NM_006895.3:c.338T>C
MANE Select
|
NP_008826.1:p.Phe113Ser
|
|