ENST00000456935.7:c.2141G>C
MANE Select
|
ENSP00000395473.2:p.Trp714Ser
|
|
ENST00000221363.8:c.2138G>C
|
ENSP00000221363.4:p.Trp713Ser
|
|
ENST00000456935.6:c.2141G>C
|
ENSP00000395473.2:p.Trp714Ser
|
|
ENST00000466794.5:n.2731G>C
|
|
|
NM_000528.3:c.2141G>C
|
NP_000519.2:p.Trp714Ser
|
|
NM_001173498.1:c.2138G>C
|
NP_001166969.1:p.Trp713Ser
|
|
XM_005259913.1:c.2144G>C
|
XP_005259970.1:p.Trp715Ser
|
|
XM_011528017.1:c.1040G>C
|
XP_011526319.1:p.Trp347Ser
|
|
XM_005259913.2:c.2144G>C
|
XP_005259970.1:p.Trp715Ser
|
|
XM_024451518.1:c.1040G>C
|
XP_024307286.1:p.Trp347Ser
|
|
NM_000528.4:c.2141G>C
MANE Select
|
NP_000519.2:p.Trp714Ser
|
|
NM_001173498.2:c.2138G>C
|
NP_001166969.1:p.Trp713Ser
|
|