ENST00000296511.10:c.21C>G
MANE Select
|
ENSP00000296511.5:p.Gly7=
|
|
ENST00000296511.9:c.21C>G
|
ENSP00000296511.5:p.Gly7=
|
|
ENST00000501272.6:c.10-2884C>G
|
ENSP00000424106.1:n.10-2884C>G
|
|
ENST00000506395.5:c.21C>G
|
ENSP00000421421.1:p.Gly7=
|
|
ENST00000509016.5:n.142C>G
|
|
|
ENST00000511552.5:n.407C>G
|
|
|
ENST00000513428.5:n.186C>G
|
|
|
ENST00000513523.1:n.189C>G
|
|
|
ENST00000513728.1:c.21C>G
|
ENSP00000427135.1:p.Gly7=
|
|
ENST00000515017.5:c.21C>G
|
ENSP00000424199.1:p.Gly7=
|
|
NM_001154.3:c.21C>G
|
NP_001145.1:p.Gly7=
|
|
XM_017008141.2:c.21C>G
|
XP_016863630.1:p.Gly7=
|
|
NM_001154.4:c.21C>G
MANE Select
|
NP_001145.1:p.Gly7=
|
|