ENST00000367698.4:c.74G=
MANE Select
|
ENSP00000356671.3:p.Gly25=
|
|
ENST00000367698.3:c.74G=
|
ENSP00000356671.3:p.Gly25=
|
|
ENST00000494024.1:n.300G=
|
|
|
ENST00000617423.4:c.74G=
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ENSP00000478688.1:p.Gly25=
|
|
NM_000488.3:c.74G= , LRG_577t1:c.74G=
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NP_000479.1:p.Gly25=
|
|
XM_005245198.2:c.-71G=
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XP_005245255.1:n.-71G=
|
|
NM_001365052.1:c.-71G=
|
NP_001351981.1:n.-71G=
|
|
NM_000488.4:c.74G=
MANE Select
|
NP_000479.1:p.Gly25=
|
|
NM_001365052.2:c.-71G=
|
NP_001351981.1:n.-71G=
|
|
NM_001386302.1:c.74G=
|
NP_001373231.1:p.Gly25=
|
|
NM_001386303.1:c.155G=
|
NP_001373232.1:p.Gly52=
|
|
NM_001386304.1:c.74G=
|
NP_001373233.1:p.Gly25=
|
|
NM_001386305.1:c.74G=
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NP_001373234.1:p.Gly25=
|
|
NM_001386306.1:c.74G=
|
NP_001373235.1:p.Gly25=
|
|