ENST00000296805.8:c.1923T>C
MANE Select
|
ENSP00000296805.3:p.Leu641=
|
|
ENST00000296805.7:c.1923T>C
|
ENSP00000296805.3:p.Leu641=
|
|
ENST00000345239.6:c.1782T>C
|
ENSP00000296804.3:p.Leu594=
|
|
ENST00000509430.5:c.1923T>C
|
ENSP00000427004.1:p.Leu641=
|
|
ENST00000514734.5:n.834T>C
|
|
|
ENST00000515125.5:n.431+196T>C
|
|
|
NM_001281302.1:c.2019T>C
|
NP_001268231.1:p.Leu673=
|
|
NM_032380.4:c.1923T>C
|
NP_115756.2:p.Leu641=
|
|
NM_170691.2:c.1782T>C
|
NP_733792.1:p.Leu594=
|
|
NR_104006.1:n.2242T>C
|
|
|
XM_006714721.2:c.1788T>C
|
XP_006714784.1:p.Leu596=
|
|
XM_011543690.1:c.1923T>C
|
XP_011541992.1:p.Leu641=
|
|
XM_017009986.1:c.1923T>C
|
XP_016865475.1:p.Leu641=
|
|
XR_002956185.1:n.3209T>C
|
|
|
NM_032380.5:c.1923T>C
MANE Select
|
NP_115756.2:p.Leu641=
|
|
NM_001281302.2:c.2019T>C
|
NP_001268231.1:p.Leu673=
|
|
NM_170691.3:c.1782T>C
|
NP_733792.1:p.Leu594=
|
|
NR_104006.2:n.1988T>C
|
|
|