ENST00000269228.10:c.57+4392A>G
MANE Select
|
ENSP00000269228.4:n.57+4392A>G
|
|
ENST00000269228.9:c.57+4392A>G
|
ENSP00000269228.4:n.57+4392A>G
|
|
ENST00000540608.5:n.201+4392A>G
|
|
|
NM_000271.4:c.57+4392A>G
|
NP_000262.2:n.57+4392A>G
|
|
XM_005258277.1:c.57+4392A>G
|
XP_005258334.1:n.57+4392A>G
|
|
XM_005258278.3:c.57+4392A>G
|
XP_005258335.1:n.57+4392A>G
|
|
XM_005258279.1:c.57+4392A>G
|
XP_005258336.1:n.57+4392A>G
|
|
XM_006722479.2:c.57+4392A>G
|
XP_006722542.1:n.57+4392A>G
|
|
XM_005258278.5:c.57+4392A>G
|
XP_005258335.1:n.57+4392A>G
|
|
XM_005258279.2:c.57+4392A>G
|
XP_005258336.1:n.57+4392A>G
|
|
XM_006722479.3:c.57+4392A>G
|
XP_006722542.1:n.57+4392A>G
|
|
XM_017025784.1:c.57+4392A>G
|
XP_016881273.1:n.57+4392A>G
|
|
XM_017025785.1:c.57+4392A>G
|
XP_016881274.1:n.57+4392A>G
|
|
XM_017025786.1:c.57+4392A>G
|
XP_016881275.1:n.57+4392A>G
|
|
XM_017025787.1:c.57+4392A>G
|
XP_016881276.1:n.57+4392A>G
|
|
NM_000271.5:c.57+4392A>G
MANE Select
|
NP_000262.2:n.57+4392A>G
|
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