ENST00000624552.4:c.14902C>G
|
ENSP00000485357.2:p.Leu4968Val
|
|
ENST00000683500.2:c.14959C>G
MANE Select
|
ENSP00000508292.2:p.Leu4987Val
|
|
ENST00000623487.1:n.3305C>G
|
|
|
ENST00000624552.3:c.14899C>G
|
ENSP00000485357.1:p.Leu4967Val
|
|
NM_001291815.1:c.14959C>G
|
NP_001278744.1:p.Leu4987Val
|
|
XM_011518465.1:c.14836C>G
|
XP_011516767.1:p.Leu4946Val
|
|
XM_011518466.1:c.14827C>G
|
XP_011516768.1:p.Leu4943Val
|
|
XM_011518467.1:c.14782C>G
|
XP_011516769.1:p.Leu4928Val
|
|
NM_001291815.2:c.14959C>G
MANE Select
|
NP_001278744.1:p.Leu4987Val
|
|
XM_011518465.2:c.14836C>G
|
XP_011516767.1:p.Leu4946Val
|
|
XM_011518466.2:c.14827C>G
|
XP_011516768.1:p.Leu4943Val
|
|
XM_011518467.2:c.14782C>G
|
XP_011516769.1:p.Leu4928Val
|
|
XM_017014585.1:c.11740C>G
|
XP_016870074.1:p.Leu3914Val
|
|
XM_017014586.1:c.7537C>G
|
XP_016870075.1:p.Leu2513Val
|
|
XR_001746957.1:n.92+209G>C
|
|
|
XR_001746958.1:n.92+209G>C
|
|
|