ENST00000265512.12:c.1016C>A
MANE Select
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ENSP00000265512.7:p.Thr339Asn
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ENST00000265512.11:c.1016C>A
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ENSP00000265512.7:p.Thr339Asn
|
|
ENST00000505590.5:c.1073C>A
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ENSP00000425416.1:p.Thr358Asn
|
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ENST00000506705.5:c.*990C>A
|
ENSP00000426667.1:n.*990C>A
|
|
ENST00000508393.5:c.1073C>A
|
ENSP00000424630.1:p.Thr358Asn
|
|
ENST00000509471.5:c.370C>A
|
ENSP00000424583.1:n.370C>A
|
|
ENST00000629236.2:c.1016C>A
|
ENSP00000486450.1:p.Thr339Asn
|
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NM_000670.3:c.1016C>A
|
NP_000661.2:p.Thr339Asn
|
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NM_000670.4:c.1016C>A
|
NP_000661.2:p.Thr339Asn
|
|
NM_001306171.1:c.1073C>A
|
NP_001293100.1:p.Thr358Asn
|
|
NM_001306172.1:c.1073C>A
|
NP_001293101.1:p.Thr358Asn
|
|
NR_037884.1:n.429-6859G>T
|
|
|
XR_938685.1:n.1244C>A
|
|
|
XR_938686.1:n.1235C>A
|
|
|
XR_938687.1:n.1108C>A
|
|
|
NM_000670.5:c.1016C>A
MANE Select
|
NP_000661.2:p.Thr339Asn
|
|
NM_001306171.2:c.1073C>A
|
NP_001293100.1:p.Thr358Asn
|
|
NM_001306172.2:c.1073C>A
|
NP_001293101.1:p.Thr358Asn
|
|