ENST00000377636.8:c.2138T>A
MANE Select
|
ENSP00000366863.3:p.Phe713Tyr
|
|
ENST00000648194.1:c.1490+1900T>A
|
ENSP00000496983.1:n.1490+1900T>A
|
|
ENST00000377625.6:c.2033+1900T>A
|
ENSP00000366852.2:n.2033+1900T>A
|
|
ENST00000377636.7:c.2138T>A
|
ENSP00000366863.3:p.Phe713Tyr
|
|
ENST00000413735.1:c.569+1900T>A
|
ENSP00000396932.1:n.569+1900T>A
|
|
ENST00000431480.6:c.2138T>A
|
ENSP00000395986.2:p.Phe713Tyr
|
|
ENST00000488955.1:n.159T>A
|
|
|
NM_001286658.1:c.2138T>A
|
NP_001273587.1:p.Phe713Tyr
|
|
NM_001286658.2:c.2138T>A
|
NP_001273587.1:p.Phe713Tyr
|
|
NM_001286659.1:c.2033+1900T>A
|
NP_001273588.1:n.2033+1900T>A
|
|
NM_001286659.2:c.2033+1900T>A
|
NP_001273588.1:n.2033+1900T>A
|
|
NM_014832.3:c.2138T>A
|
NP_055647.2:p.Phe713Tyr
|
|
NM_014832.4:c.2138T>A
|
NP_055647.2:p.Phe713Tyr
|
|
XM_005266603.1:c.2063T>A
|
XP_005266660.1:p.Phe688Tyr
|
|
XM_005266605.1:c.1595T>A
|
XP_005266662.1:p.Phe532Tyr
|
|
XM_006719903.2:c.1664T>A
|
XP_006719966.1:p.Phe555Tyr
|
|
XM_011535331.1:c.2027T>A
|
XP_011533633.1:p.Phe676Tyr
|
|
XM_005266603.2:c.2063T>A
|
XP_005266660.1:p.Phe688Tyr
|
|
XM_005266605.3:c.1595T>A
|
XP_005266662.1:p.Phe532Tyr
|
|
XM_006719903.3:c.1664T>A
|
XP_006719966.1:p.Phe555Tyr
|
|
XM_011535331.2:c.2027T>A
|
XP_011533633.1:p.Phe676Tyr
|
|
XM_017020882.2:c.1490+1900T>A
|
XP_016876371.1:n.1490+1900T>A
|
|
XM_017020883.2:c.1379+1900T>A
|
XP_016876372.1:n.1379+1900T>A
|
|
NM_014832.5:c.2138T>A
MANE Select
|
NP_055647.2:p.Phe713Tyr
|
|