ENST00000368407.8:c.496C>G
MANE Select
|
ENSP00000357392.3:p.Leu166Val
|
|
ENST00000368406.2:c.430C>G
|
ENSP00000357391.2:p.Leu144Val
|
|
ENST00000368407.7:c.496C>G
|
ENSP00000357392.3:p.Leu166Val
|
|
ENST00000469878.5:n.747C>G
|
|
|
ENST00000474413.5:n.721C>G
|
|
|
ENST00000497282.1:n.539C>G
|
|
|
NM_004428.2:c.496C>G
|
NP_004419.2:p.Leu166Val
|
|
NM_182685.1:c.430C>G
|
NP_872626.1:p.Leu144Val
|
|
XM_005244940.3:c.307C>G
|
XP_005244997.1:p.Leu103Val
|
|
NM_004428.3:c.496C>G
MANE Select
|
NP_004419.2:p.Leu166Val
|
|
NM_182685.2:c.430C>G
|
NP_872626.1:p.Leu144Val
|
|