ENST00000216802.10:c.59T>C
MANE Select
|
ENSP00000216802.5:p.Phe20Ser
|
|
ENST00000216802.9:c.59T>C
|
ENSP00000216802.5:p.Phe20Ser
|
|
ENST00000471700.6:n.57T>C
|
|
|
ENST00000558273.5:c.59T>C
|
ENSP00000453195.1:p.Phe20Ser
|
|
ENST00000558931.5:n.736T>C
|
|
|
ENST00000559056.5:c.-173T>C
|
ENSP00000452940.1:n.-173T>C
|
|
ENST00000559453.5:n.9T>C
|
|
|
ENST00000559493.5:n.56T>C
|
|
|
ENST00000559613.1:n.107T>C
|
|
|
ENST00000560370.3:c.59T>C
|
ENSP00000453161.1:p.Phe20Ser
|
|
ENST00000560410.5:c.48+304T>C
|
ENSP00000453487.1:n.48+304T>C
|
|
ENST00000560592.5:n.99T>C
|
|
|
ENST00000560788.1:n.74T>C
|
|
|
ENST00000615264.4:c.59T>C
|
ENSP00000484569.1:p.Phe20Ser
|
|
ENST00000630027.1:c.59T>C
|
ENSP00000485798.1:p.Phe20Ser
|
|
NM_002818.2:c.59T>C
|
NP_002809.2:p.Phe20Ser
|
|
XM_006720213.1:c.-297T>C
|
XP_006720276.1:n.-297T>C
|
|
XM_006720213.2:c.-297T>C
|
XP_006720276.1:n.-297T>C
|
|
NM_002818.3:c.59T>C
MANE Select
|
NP_002809.2:p.Phe20Ser
|
|