|
NM_012464.5:c.2424T>C
MANE Select
|
NP_036596.3:p.Pro808=
|
|
ENST00000061240.7:c.2424T>C
MANE Select
|
ENSP00000061240.2:p.Pro808=
|
|
NM_012464.4:c.2424T>C
|
NP_036596.3:p.Pro808=
|
|
ENST00000061240.6:c.2424T>C
|
ENSP00000061240.2:p.Pro808=
|
|
ENST00000507499.5:c.2493T>C
|
ENSP00000426082.1:p.Pro831=
|
|
ENST00000509505.5:c.*2069T>C
|
ENSP00000422692.1:n.*2069T>C
|
|
XM_011532212.1:c.2508T>C
|
XP_011530514.1:p.Pro836=
|
|
XM_011532213.1:c.2361T>C
|
XP_011530515.1:p.Pro787=
|
|
XM_011532214.1:c.1896T>C
|
XP_011530516.1:p.Pro632=
|
|
XM_017008570.1:c.2277T>C
|
XP_016864059.1:p.Pro759=
|
|
XM_024454194.1:c.2124T>C
|
XP_024309962.1:p.Pro708=
|
|
XM_024454195.1:c.2124T>C
|
XP_024309963.1:p.Pro708=
|