ENST00000216341.9:c.151G=
MANE Select
|
ENSP00000216341.4:p.Gly51=
|
|
ENST00000216341.8:c.151G=
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ENSP00000216341.4:p.Gly51=
|
|
ENST00000382540.5:c.151G=
|
ENSP00000371980.1:p.Gly51=
|
|
ENST00000382542.5:c.151G=
|
ENSP00000371982.2:p.Gly51=
|
|
ENST00000415355.7:c.115G=
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ENSP00000387385.3:p.Gly39=
|
|
ENST00000526004.1:c.151G=
|
ENSP00000434213.1:p.Gly51=
|
|
ENST00000530830.1:c.*74G=
|
ENSP00000435084.1:n.*74G=
|
|
ENST00000532263.5:c.56-849G=
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ENSP00000432074.1:n.56-849G=
|
|
ENST00000554242.5:c.151G=
|
ENSP00000450535.1:p.Gly51=
|
|
ENST00000616551.1:c.52-846G=
|
ENSP00000479643.1:n.52-846G=
|
|
NM_004131.4:c.151G=
|
NP_004122.2:p.Gly51=
|
|
XM_011536685.1:c.115G=
|
XP_011534987.1:p.Gly39=
|
|
NM_001346011.1:c.115G=
|
NP_001332940.1:p.Gly39=
|
|
NM_004131.5:c.151G=
|
NP_004122.2:p.Gly51=
|
|
NR_144343.1:n.260G=
|
|
|
NM_004131.6:c.151G=
MANE Select
|
NP_004122.2:p.Gly51=
|
|
NM_001346011.2:c.115G=
|
NP_001332940.1:p.Gly39=
|
|
NR_144343.2:n.181G=
|
|
|