ENST00000296674.13:c.271T>G
(RPS23)
MANE Select
|
ENSP00000296674.8:p.Leu91Val
|
|
ENST00000651545.1:c.271T>G
(RPS23)
|
ENSP00000498621.1:p.Leu91Val
|
|
ENST00000296674.12:c.271T>G
(RPS23)
|
ENSP00000296674.8:p.Leu91Val
|
|
ENST00000503605.1:n.480T>G
(RPS23)
|
|
|
ENST00000504293.5:n.366T>G
(RPS23)
|
|
|
ENST00000507980.1:c.271T>G
(RPS23)
|
ENSP00000422071.1:p.Leu91Val
|
|
ENST00000510019.5:c.232+39T>G
(RPS23)
|
ENSP00000425833.1:n.232+39T>G
|
|
ENST00000510210.5:c.271T>G
(RPS23)
|
ENSP00000427043.1:p.Leu91Val
|
|
ENST00000512493.5:c.271T>G
(RPS23)
|
ENSP00000425865.1:p.Leu91Val
|
|
ENST00000514253.2:n.459A>C
(ATG10)
|
|
|
NM_001025.4:c.271T>G
(RPS23)
|
NP_001016.1:p.Leu91Val
|
|
NM_001025.5:c.271T>G
(RPS23)
MANE Select
|
NP_001016.1:p.Leu91Val
|
|