ENST00000388913.4:c.1163G>C
MANE Select
|
ENSP00000373565.3:p.Gly388Ala
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ENST00000650760.1:c.1766G>C
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ENSP00000499217.1:p.Gly589Ala
|
|
ENST00000388913.3:c.1163G>C
|
ENSP00000373565.3:p.Gly388Ala
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ENST00000395103.2:c.343G>C
|
|
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NM_198488.3:c.1163G>C
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NP_940890.3:p.Gly388Ala
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XM_005250887.2:c.1220G>C
|
XP_005250944.1:p.Gly407Ala
|
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XM_005250888.2:c.1181G>C
|
XP_005250945.1:p.Gly394Ala
|
|
XM_005250889.2:c.1163G>C
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XP_005250946.1:p.Gly388Ala
|
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XM_011516980.1:c.1484G>C
|
XP_011515282.1:p.Gly495Ala
|
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XM_011516981.1:c.1331G>C
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XP_011515283.1:p.Gly444Ala
|
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XM_005250887.3:c.1220G>C
|
XP_005250944.1:p.Gly407Ala
|
|
XM_005250888.3:c.1181G>C
|
XP_005250945.1:p.Gly394Ala
|
|
XM_005250889.3:c.1163G>C
|
XP_005250946.1:p.Gly388Ala
|
|
XM_011516980.2:c.1766G>C
|
XP_011515282.2:p.Gly589Ala
|
|
XM_011516981.2:c.1331G>C
|
XP_011515283.1:p.Gly444Ala
|
|
XM_024447131.1:c.1163G>C
|
XP_024302899.1:p.Gly388Ala
|
|
NM_198488.4:c.1163G>C
|
NP_940890.3:p.Gly388Ala
|
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NM_198488.5:c.1163G>C
MANE Select
|
NP_940890.4:p.Gly388Ala
|
|