ENST00000706528.1:n.1455T>G
|
|
|
ENST00000240306.5:c.574T>G
MANE Select
|
ENSP00000240306.3:p.Phe192Val
|
|
ENST00000240306.4:c.574T>G
|
ENSP00000240306.3:p.Phe192Val
|
|
ENST00000411890.3:c.358T>G
|
ENSP00000410622.2:p.Phe120Val
|
|
ENST00000611342.1:c.*444T>G
|
ENSP00000480366.1:n.*444T>G
|
|
NM_001934.3:c.358T>G
|
NP_001925.2:p.Phe120Val
|
|
NM_138281.2:c.574T>G
|
NP_612138.1:p.Phe192Val
|
|
XM_011524459.1:c.358T>G
|
XP_011522761.1:p.Phe120Val
|
|
XM_017024291.1:c.358T>G
|
XP_016879780.1:p.Phe120Val
|
|
NM_138281.3:c.574T>G
MANE Select
|
NP_612138.1:p.Phe192Val
|
|
NM_001934.4:c.358T>G
|
NP_001925.2:p.Phe120Val
|
|