ENST00000646743.1:c.118T=
MANE Select
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ENSP00000495564.1:p.Leu40=
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|
ENST00000251808.7:c.118T=
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ENSP00000251808.3:p.Leu40=
|
|
ENST00000395927.1:c.70T=
|
ENSP00000379260.1:p.Leu24=
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|
ENST00000472106.2:n.446T=
|
|
|
NM_024915.3:c.118T=
|
NP_079191.2:p.Leu40=
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|
XM_011517305.1:c.70T=
|
XP_011515607.1:p.Leu24=
|
|
XM_011517306.1:c.70T=
|
XP_011515608.1:p.Leu24=
|
|
XM_011517307.1:c.118T=
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XP_011515609.1:p.Leu40=
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|
NM_001330593.1:c.70T=
|
NP_001317522.1:p.Leu24=
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|
XM_011517306.3:c.70T=
|
XP_011515608.1:p.Leu24=
|
|
XM_011517307.3:c.118T=
|
XP_011515609.1:p.Leu40=
|
|
NM_001330593.2:c.70T=
|
NP_001317522.1:p.Leu24=
|
|
NM_024915.4:c.118T=
MANE Select
|
NP_079191.2:p.Leu40=
|
|