ENST00000378802.5:c.1189T>G
MANE Select
|
ENSP00000368079.4:p.Leu397Val
|
|
ENST00000378802.4:c.1189T>G
|
ENSP00000368079.4:p.Leu397Val
|
|
ENST00000502665.1:n.424T>G
|
|
|
ENST00000507209.5:n.5887T>G
|
|
|
ENST00000513354.5:n.279T>G
|
|
|
NM_207352.3:c.1189T>G
|
NP_997235.3:p.Leu397Val
|
|
XM_005262935.2:c.1189T>G
|
XP_005262992.1:p.Leu397Val
|
|
XM_006714184.2:c.793T>G
|
XP_006714247.1:p.Leu265Val
|
|
XM_005262935.4:c.1189T>G
|
XP_005262992.1:p.Leu397Val
|
|
XM_017008037.1:c.793T>G
|
XP_016863526.1:p.Leu265Val
|
|
NM_207352.4:c.1189T>G
MANE Select
|
NP_997235.3:p.Leu397Val
|
|