ENST00000367698.4:c.941T>G
MANE Select
|
ENSP00000356671.3:p.Val314Gly
|
|
ENST00000367698.3:c.941T>G
|
ENSP00000356671.3:p.Val314Gly
|
|
ENST00000487183.1:n.592T>G
|
|
|
ENST00000617423.4:c.559+2100T>G
|
ENSP00000478688.1:n.559+2100T>G
|
|
NM_000488.3:c.941T>G , LRG_577t1:c.941T>G
|
NP_000479.1:p.Val314Gly
|
|
XM_005245198.2:c.797T>G
|
XP_005245255.1:p.Val266Gly
|
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NM_001365052.1:c.797T>G
|
NP_001351981.1:p.Val266Gly
|
|
NM_000488.4:c.941T>G
MANE Select
|
NP_000479.1:p.Val314Gly
|
|
NM_001365052.2:c.797T>G
|
NP_001351981.1:p.Val266Gly
|
|
NM_001386302.1:c.1064T>G
|
NP_001373231.1:p.Val355Gly
|
|
NM_001386303.1:c.1022T>G
|
NP_001373232.1:p.Val341Gly
|
|
NM_001386304.1:c.920T>G
|
NP_001373233.1:p.Val307Gly
|
|
NM_001386305.1:c.884T>G
|
NP_001373234.1:p.Val295Gly
|
|
NM_001386306.1:c.725T>G
|
NP_001373235.1:p.Val242Gly
|
|