ENST00000433957.7:c.904G>T
|
ENSP00000411013.3:p.Gly302Cys
|
|
ENST00000644384.2:c.904G>T
MANE Select
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ENSP00000494414.1:p.Gly302Cys
|
|
ENST00000652415.1:c.904G>T
|
ENSP00000498756.1:p.Gly302Cys
|
|
ENST00000291532.7:c.904G>T
|
ENSP00000291532.3:p.Gly302Cys
|
|
ENST00000398397.3:c.904G>T
|
ENSP00000381434.3:p.Gly302Cys
|
|
ENST00000398405.5:c.898G>T
|
ENSP00000381442.1:p.Gly300Cys
|
|
ENST00000433957.6:c.904G>T
|
ENSP00000411013.2:p.Gly302Cys
|
|
ENST00000474596.5:n.772G>T
|
|
|
ENST00000476848.5:n.1639G>T
|
|
|
ENST00000478680.1:n.181G>T
|
|
|
ENST00000482761.1:n.1191G>T
|
|
|
NM_001256317.1:c.904G>T
|
NP_001243246.1:p.Gly302Cys
|
|
NM_024022.2:c.904G>T
|
NP_076927.1:p.Gly302Cys
|
|
NM_032404.2:c.523G>T
|
NP_115780.1:p.Gly175Cys
|
|
NM_032405.1:c.904G>T
|
NP_115781.1:p.Gly302Cys
|
|
NR_046020.1:n.1860G>T
|
|
|
NM_001256317.2:c.904G>T
|
NP_001243246.1:p.Gly302Cys
|
|
NM_024022.3:c.904G>T
|
NP_076927.1:p.Gly302Cys
|
|
NM_032405.2:c.904G>T
|
NP_115781.1:p.Gly302Cys
|
|
NM_001256317.3:c.904G>T
MANE Select
|
NP_001243246.1:p.Gly302Cys
|
|
NM_024022.4:c.904G>T
|
NP_076927.1:p.Gly302Cys
|
|
NM_032404.3:c.523G>T
|
NP_115780.1:p.Gly175Cys
|
|