ENST00000614874.2:c.445_446delinsGC
|
ENSP00000507272.1:p.Ala149=
|
|
ENST00000682620.1:n.1631-541_1631-540delinsGC
|
|
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ENST00000684771.1:n.585-541_585-540delinsGC
|
|
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ENST00000228872.9:c.445_446delinsGC
MANE Select
|
ENSP00000228872.4:p.Ala149=
|
|
ENST00000228872.8:c.445_446delinsGC
|
ENSP00000228872.4:p.Ala149=
|
|
ENST00000396340.1:c.445_446delinsGC
|
ENSP00000379629.1:p.Ala149=
|
|
ENST00000442489.1:c.193+231_193+232delinsGC
|
ENSP00000407597.1:n.193+231_193+232delinsGC
|
|
ENST00000477087.1:n.155-541_155-540delinsGC
|
|
|
NM_004064.4:c.445_446delinsGC
|
NP_004055.1:p.Ala149=
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|
NM_004064.5:c.445_446delinsGC
MANE Select
|
NP_004055.1:p.Ala149=
|
|