ENST00000272286.4:c.1805G>C
MANE Select
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ENSP00000272286.2:p.Gly602Ala
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ENST00000272286.2:c.1805G>C
|
ENSP00000272286.2:p.Gly602Ala
|
|
NM_022437.2:c.1805G>C
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NP_071882.1:p.Gly602Ala
|
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XM_005264483.2:c.1802G>C
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XP_005264540.1:p.Gly601Ala
|
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XM_011533029.1:c.1817G>C
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XP_011531331.1:p.Gly606Ala
|
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XM_011533030.1:c.1814G>C
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XP_011531332.1:p.Gly605Ala
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XM_011533031.1:c.1589G>C
|
XP_011531333.1:p.Gly530Ala
|
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XR_939707.1:n.2307G>C
|
|
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NM_001357321.1:c.1802G>C
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NP_001344250.1:p.Gly601Ala
|
|
XM_011533029.2:c.1817G>C
|
XP_011531331.1:p.Gly606Ala
|
|
XM_011533030.2:c.1814G>C
|
XP_011531332.1:p.Gly605Ala
|
|
XR_001738891.1:n.2321G>C
|
|
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XR_939707.2:n.2321G>C
|
|
|
NM_022437.3:c.1805G>C
MANE Select
|
NP_071882.1:p.Gly602Ala
|
|
NM_001357321.2:c.1802G>C
|
NP_001344250.1:p.Gly601Ala
|
|