ENST00000378802.5:c.1092G>A
MANE Select
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ENSP00000368079.4:p.Gly364=
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|
ENST00000378802.4:c.1092G>A
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ENSP00000368079.4:p.Gly364=
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ENST00000502665.1:n.327G>A
|
|
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ENST00000507209.5:n.5790G>A
|
|
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ENST00000513354.5:n.182G>A
|
|
|
NM_207352.3:c.1092G>A
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NP_997235.3:p.Gly364=
|
|
XM_005262935.2:c.1092G>A
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XP_005262992.1:p.Gly364=
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XM_006714184.2:c.696G>A
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XP_006714247.1:p.Gly232=
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XM_005262935.4:c.1092G>A
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XP_005262992.1:p.Gly364=
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XM_017008037.1:c.696G>A
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XP_016863526.1:p.Gly232=
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NM_207352.4:c.1092G>A
MANE Select
|
NP_997235.3:p.Gly364=
|
|