ENST00000355832.10:c.3889C>G
MANE Select
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ENSP00000348089.5:p.Leu1297Val
|
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ENST00000679552.1:n.960C>G
|
|
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ENST00000679871.1:n.1035C>G
|
|
|
ENST00000679974.1:n.938C>G
|
|
|
ENST00000681632.1:n.5292C>G
|
|
|
ENST00000681659.1:c.3730C>G
|
ENSP00000505631.1:p.Leu1244Val
|
|
ENST00000355832.9:c.3889C>G
|
ENSP00000348089.5:p.Leu1297Val
|
|
ENST00000465653.1:n.211C>G
|
|
|
ENST00000623073.3:c.*2185C>G
|
ENSP00000485650.1:n.*2185C>G
|
|
ENST00000623115.3:c.1999C>G
|
ENSP00000485321.1:p.Leu667Val
|
|
ENST00000624341.3:c.1721C>G
|
|
|
NM_000124.3:c.3889C>G
|
NP_000115.1:p.Leu1297Val
|
|
XR_945953.1:n.243-10119G>C
|
|
|
NM_001346440.1:c.3889C>G
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NP_001333369.1:p.Leu1297Val
|
|
NM_000124.4:c.3889C>G
MANE Select
|
NP_000115.1:p.Leu1297Val
|
|
NM_001346440.2:c.3889C>G
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NP_001333369.1:p.Leu1297Val
|
|