ENST00000573725.2:c.6779T=
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ENSP00000460849.2:p.Leu2260=
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|
ENST00000703537.1:c.2707T=
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|
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ENST00000703538.1:c.*6682T=
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ENSP00000515361.1:n.*6682T=
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ENST00000703539.1:n.3273T=
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|
|
ENST00000703540.1:c.6812T=
|
ENSP00000515362.1:p.Leu2271=
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ENST00000703541.1:c.6824T=
|
ENSP00000515363.1:p.Leu2275=
|
|
ENST00000304992.11:c.6959T=
MANE Select
|
ENSP00000304350.6:p.Leu2320=
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ENST00000304992.10:c.6959T=
|
ENSP00000304350.6:p.Leu2320=
|
|
ENST00000571958.1:c.163-5T=
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|
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ENST00000572621.5:c.6959T=
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ENSP00000460348.1:p.Leu2320=
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|
ENST00000572723.1:n.948T=
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|
|
NM_006445.3:c.6959T=
|
NP_006436.3:p.Leu2320=
|
|
XM_024450537.1:c.6959T=
|
XP_024306305.1:p.Leu2320=
|
|
NM_006445.4:c.6959T=
MANE Select
|
NP_006436.3:p.Leu2320=
|
|