ENST00000265104.5:c.12613G>T
MANE Select
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ENSP00000265104.4:p.Gly4205Trp
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|
ENST00000681290.1:c.12568G>T
|
ENSP00000505288.1:p.Gly4190Trp
|
|
ENST00000265104.4:c.12613G>T
|
ENSP00000265104.4:p.Gly4205Trp
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NM_001369.2:c.12613G>T
|
NP_001360.1:p.Gly4205Trp
|
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XM_005248262.2:c.12568G>T
|
XP_005248319.1:p.Gly4190Trp
|
|
XM_005248262.3:c.12721G>T
|
XP_005248319.2:p.Gly4241Trp
|
|
XM_017009177.1:c.12721G>T
|
XP_016864666.1:p.Gly4241Trp
|
|
XM_017009178.1:c.11626G>T
|
XP_016864667.1:p.Gly3876Trp
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XM_017009179.2:c.11626G>T
|
XP_016864668.1:p.Gly3876Trp
|
|
XM_017009180.1:c.12721G>T
|
XP_016864669.1:p.Gly4241Trp
|
|
XM_017009185.1:c.7810G>T
|
XP_016864674.1:p.Gly2604Trp
|
|
XM_017009186.1:c.7363G>T
|
XP_016864675.1:p.Gly2455Trp
|
|
XM_017009188.1:c.6700G>T
|
XP_016864677.1:p.Gly2234Trp
|
|
XM_024454388.1:c.11626G>T
|
XP_024310156.1:p.Gly3876Trp
|
|
XM_024454389.1:c.11215G>T
|
XP_024310157.1:p.Gly3739Trp
|
|
NM_001369.3:c.12613G>T
MANE Select
|
NP_001360.1:p.Gly4205Trp
|
|