ENST00000433957.7:c.871G>T
|
ENSP00000411013.3:p.Val291Phe
|
|
ENST00000644384.2:c.871G>T
MANE Select
|
ENSP00000494414.1:p.Val291Phe
|
|
ENST00000652415.1:c.871G>T
|
ENSP00000498756.1:p.Val291Phe
|
|
ENST00000291532.7:c.871G>T
|
ENSP00000291532.3:p.Val291Phe
|
|
ENST00000398397.3:c.871G>T
|
ENSP00000381434.3:p.Val291Phe
|
|
ENST00000398405.5:c.865G>T
|
ENSP00000381442.1:p.Val289Phe
|
|
ENST00000433957.6:c.871G>T
|
ENSP00000411013.2:p.Val291Phe
|
|
ENST00000474596.5:n.739G>T
|
|
|
ENST00000476848.5:n.1606G>T
|
|
|
ENST00000478680.1:n.148G>T
|
|
|
ENST00000482761.1:n.1158G>T
|
|
|
NM_001256317.1:c.871G>T
|
NP_001243246.1:p.Val291Phe
|
|
NM_024022.2:c.871G>T
|
NP_076927.1:p.Val291Phe
|
|
NM_032404.2:c.490G>T
|
NP_115780.1:p.Val164Phe
|
|
NM_032405.1:c.871G>T
|
NP_115781.1:p.Val291Phe
|
|
NR_046020.1:n.1827G>T
|
|
|
NM_001256317.2:c.871G>T
|
NP_001243246.1:p.Val291Phe
|
|
NM_024022.3:c.871G>T
|
NP_076927.1:p.Val291Phe
|
|
NM_032405.2:c.871G>T
|
NP_115781.1:p.Val291Phe
|
|
NM_001256317.3:c.871G>T
MANE Select
|
NP_001243246.1:p.Val291Phe
|
|
NM_024022.4:c.871G>T
|
NP_076927.1:p.Val291Phe
|
|
NM_032404.3:c.490G>T
|
NP_115780.1:p.Val164Phe
|
|