ENST00000262493.12:c.775T>C
MANE Select
|
ENSP00000262493.6:p.Phe259Leu
|
|
ENST00000562316.6:c.442T>C
|
ENSP00000457238.2:p.Phe148Leu
|
|
ENST00000564727.2:c.79T>C
|
ENSP00000454971.2:p.Phe27Leu
|
|
ENST00000568375.2:c.116-3431T>C
|
|
|
ENST00000638185.1:n.990T>C
|
|
|
ENST00000638210.1:n.1075T>C
|
|
|
ENST00000638705.1:c.775T>C
|
ENSP00000491223.1:p.Phe259Leu
|
|
ENST00000638836.1:n.685T>C
|
|
|
ENST00000639055.1:n.1496T>C
|
|
|
ENST00000639251.1:n.676T>C
|
|
|
ENST00000639268.1:c.410T>C
|
|
|
ENST00000639341.1:c.300T>C
|
|
|
ENST00000639770.1:c.813T>C
|
ENSP00000491999.1:n.813T>C
|
|
ENST00000640390.1:n.705T>C
|
|
|
ENST00000640469.1:c.139T>C
|
ENSP00000491875.1:p.Phe47Leu
|
|
ENST00000640560.1:n.551T>C
|
|
|
ENST00000640893.1:c.*173T>C
|
ENSP00000492677.1:n.*173T>C
|
|
ENST00000262493.10:c.775T>C
|
ENSP00000262493.6:p.Phe259Leu
|
|
ENST00000568375.1:n.116-3431T>C
|
|
|
NM_020988.2:c.775T>C
|
NP_066268.1:p.Phe259Leu
|
|
XM_011523003.1:c.649T>C
|
XP_011521305.1:p.Phe217Leu
|
|
XM_011523003.3:c.649T>C
|
XP_011521305.1:p.Phe217Leu
|
|
NM_020988.3:c.775T>C
MANE Select
|
NP_066268.1:p.Phe259Leu
|
|