ENST00000265104.5:c.12604G>T
MANE Select
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ENSP00000265104.4:p.Gly4202Cys
|
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ENST00000681290.1:c.12559G>T
|
ENSP00000505288.1:p.Gly4187Cys
|
|
ENST00000265104.4:c.12604G>T
|
ENSP00000265104.4:p.Gly4202Cys
|
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NM_001369.2:c.12604G>T
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NP_001360.1:p.Gly4202Cys
|
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XM_005248262.2:c.12559G>T
|
XP_005248319.1:p.Gly4187Cys
|
|
XM_005248262.3:c.12712G>T
|
XP_005248319.2:p.Gly4238Cys
|
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XM_017009177.1:c.12712G>T
|
XP_016864666.1:p.Gly4238Cys
|
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XM_017009178.1:c.11617G>T
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XP_016864667.1:p.Gly3873Cys
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XM_017009179.2:c.11617G>T
|
XP_016864668.1:p.Gly3873Cys
|
|
XM_017009180.1:c.12712G>T
|
XP_016864669.1:p.Gly4238Cys
|
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XM_017009185.1:c.7801G>T
|
XP_016864674.1:p.Gly2601Cys
|
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XM_017009186.1:c.7354G>T
|
XP_016864675.1:p.Gly2452Cys
|
|
XM_017009188.1:c.6691G>T
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XP_016864677.1:p.Gly2231Cys
|
|
XM_024454388.1:c.11617G>T
|
XP_024310156.1:p.Gly3873Cys
|
|
XM_024454389.1:c.11206G>T
|
XP_024310157.1:p.Gly3736Cys
|
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NM_001369.3:c.12604G>T
MANE Select
|
NP_001360.1:p.Gly4202Cys
|
|