ENST00000355832.10:c.3896T>C
MANE Select
|
ENSP00000348089.5:p.Leu1299Pro
|
|
ENST00000679552.1:n.967T>C
|
|
|
ENST00000679871.1:n.1042T>C
|
|
|
ENST00000679974.1:n.945T>C
|
|
|
ENST00000681632.1:n.5299T>C
|
|
|
ENST00000681659.1:c.3737T>C
|
ENSP00000505631.1:p.Leu1246Pro
|
|
ENST00000355832.9:c.3896T>C
|
ENSP00000348089.5:p.Leu1299Pro
|
|
ENST00000465653.1:n.218T>C
|
|
|
ENST00000623073.3:c.*2192T>C
|
ENSP00000485650.1:n.*2192T>C
|
|
ENST00000623115.3:c.2006T>C
|
ENSP00000485321.1:p.Leu669Pro
|
|
ENST00000624341.3:c.1728T>C
|
|
|
NM_000124.3:c.3896T>C
|
NP_000115.1:p.Leu1299Pro
|
|
XR_945953.1:n.243-10126A>G
|
|
|
NM_001346440.1:c.3896T>C
|
NP_001333369.1:p.Leu1299Pro
|
|
NM_000124.4:c.3896T>C
MANE Select
|
NP_000115.1:p.Leu1299Pro
|
|
NM_001346440.2:c.3896T>C
|
NP_001333369.1:p.Leu1299Pro
|
|