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NM_000088.4:c.4081G>C
MANE Select
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NP_000079.2:p.Glu1361Gln
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|
ENST00000225964.10:c.4081G>C
MANE Select
|
ENSP00000225964.6:p.Glu1361Gln
|
|
NM_000088.3:c.4081G>C , LRG_1t1:c.4081G>C
|
NP_000079.2:p.Glu1361Gln
|
|
ENST00000225964.9:c.4081G>C
|
ENSP00000225964.5:p.Glu1361Gln
|
|
ENST00000510710.3:n.1046G>C
|
|
|
XM_005257058.3:c.3811G>C
|
XP_005257115.2:p.Glu1271Gln
|
|
XM_005257058.4:c.3811G>C
|
XP_005257115.2:p.Glu1271Gln
|
|
XM_005257059.3:c.3163G>C
|
XP_005257116.2:p.Glu1055Gln
|
|
XM_005257059.4:c.3163G>C
|
XP_005257116.2:p.Glu1055Gln
|
|
XM_011524341.1:c.3883G>C
|
XP_011522643.1:p.Glu1295Gln
|