ENST00000696156.1:c.469G>T
|
ENSP00000512446.1:p.Val157Phe
|
|
ENST00000696157.1:c.*770G>T
|
ENSP00000512447.1:n.*770G>T
|
|
ENST00000696158.1:c.*807G>T
|
ENSP00000512448.1:n.*807G>T
|
|
ENST00000696159.1:c.*476G>T
|
ENSP00000512449.1:n.*476G>T
|
|
ENST00000696160.1:c.580G>T
|
ENSP00000512450.1:p.Val194Phe
|
|
ENST00000696161.1:c.683G>T
|
ENSP00000512451.1:p.Gly228Val
|
|
ENST00000696162.1:c.*1272G>T
|
ENSP00000512452.1:n.*1272G>T
|
|
ENST00000696163.1:c.502G>T
|
ENSP00000512453.1:p.Val168Phe
|
|
ENST00000261623.8:c.553G>T
MANE Select
|
ENSP00000261623.3:p.Val185Phe
|
|
ENST00000261623.7:c.553G>T
|
ENSP00000261623.3:p.Val185Phe
|
|
NM_000101.3:c.553G>T
|
NP_000092.2:p.Val185Phe
|
|
NM_000101.4:c.553G>T
MANE Select
|
NP_000092.2:p.Val185Phe
|
|