ENST00000426263.10:c.687G>C
MANE Select
|
ENSP00000416293.2:p.Lys229Asn
|
|
ENST00000669445.1:c.57-40G>C
|
|
|
ENST00000674765.1:c.687G>C
|
ENSP00000501811.1:p.Lys229Asn
|
|
ENST00000675112.1:n.710G>C
|
|
|
ENST00000676254.1:n.1136G>C
|
|
|
ENST00000426263.7:c.687G>C
|
ENSP00000416293.2:p.Lys229Asn
|
|
ENST00000439722.2:c.566G>C
|
ENSP00000395521.2:n.566G>C
|
|
ENST00000475162.3:c.415+853G>C
|
|
|
ENST00000630287.2:c.*2G>C
|
ENSP00000486694.1:n.*2G>C
|
|
NM_006516.2:c.687G>C
|
NP_006507.2:p.Lys229Asn
|
|
NM_006516.3:c.687G>C
|
NP_006507.2:p.Lys229Asn
|
|
NM_006516.4:c.687G>C
MANE Select
|
NP_006507.2:p.Lys229Asn
|
|