ENST00000259407.7:c.964T>G
MANE Select
|
ENSP00000259407.2:p.Phe322Val
|
|
ENST00000395051.4:c.964T>G
|
ENSP00000378491.3:p.Phe322Val
|
|
ENST00000674556.1:c.964T>G
|
ENSP00000501610.1:p.Phe322Val
|
|
ENST00000674791.1:c.762+202T>G
|
ENSP00000501644.1:n.762+202T>G
|
|
ENST00000674909.1:c.804+160T>G
|
ENSP00000502812.1:n.804+160T>G
|
|
ENST00000259407.6:c.964T>G
|
ENSP00000259407.2:p.Phe322Val
|
|
ENST00000395051.3:c.964T>G
|
ENSP00000378491.3:p.Phe322Val
|
|
NM_001127610.1:c.964T>G
|
NP_001121082.1:p.Phe322Val
|
|
NM_001701.3:c.964T>G
|
NP_001692.1:p.Phe322Val
|
|
NM_001127610.2:c.964T>G
|
NP_001121082.1:p.Phe322Val
|
|
NM_001374715.1:c.964T>G
|
NP_001361644.1:p.Phe322Val
|
|
NM_001701.4:c.964T>G
MANE Select
|
NP_001692.1:p.Phe322Val
|
|