ENST00000317447.9:c.1682T>C
|
ENSP00000320646.4:p.Met561Thr
|
|
ENST00000614302.5:c.1682T>C
MANE Select
|
ENSP00000479130.1:p.Met561Thr
|
|
ENST00000649953.1:c.1892T>C
|
ENSP00000497456.1:p.Met631Thr
|
|
ENST00000317447.8:c.1682T>C
|
ENSP00000320646.4:p.Met561Thr
|
|
ENST00000378345.8:c.887T>C
|
ENSP00000367596.4:p.Met296Thr
|
|
ENST00000393145.5:n.6592T>C
|
|
|
ENST00000406948.7:c.1682T>C
|
ENSP00000384627.3:p.Met561Thr
|
|
ENST00000537116.5:n.808T>C
|
|
|
ENST00000537155.1:n.422T>C
|
|
|
ENST00000542688.5:c.*426T>C
|
ENSP00000446281.1:n.*426T>C
|
|
ENST00000614302.4:c.1682T>C
|
ENSP00000479130.1:p.Met561Thr
|
|
NM_001127214.3:c.1682T>C
|
NP_001120686.1:p.Met561Thr
|
|
NM_001243279.2:c.1682T>C
|
NP_001230208.1:p.Met561Thr
|
|
NM_001284316.1:c.887T>C
|
NP_001271245.1:p.Met296Thr
|
|
NM_174917.4:c.1682T>C
|
NP_777577.2:p.Met561Thr
|
|
NR_045667.2:n.808T>C
|
|
|
NR_104293.1:n.2116T>C
|
|
|
XR_933239.1:n.2123T>C
|
|
|
XR_933240.1:n.2120T>C
|
|
|
XR_933241.1:n.1877T>C
|
|
|
NR_147928.1:n.2160T>C
|
|
|
NR_147929.1:n.1914T>C
|
|
|
XM_017023020.2:c.-3423T>C
|
XP_016878509.1:n.-3423T>C
|
|
XM_024450187.1:c.887T>C
|
XP_024305955.1:p.Met296Thr
|
|
XR_001751864.2:n.1929T>C
|
|
|
XR_933240.3:n.2119T>C
|
|
|
NM_001127214.4:c.1682T>C
|
NP_001120686.1:p.Met561Thr
|
|
NM_001243279.3:c.1682T>C
MANE Select
|
NP_001230208.1:p.Met561Thr
|
|
NM_001284316.2:c.887T>C
|
NP_001271245.1:p.Met296Thr
|
|
NM_174917.5:c.1682T>C
|
NP_777577.2:p.Met561Thr
|
|
NR_104293.2:n.2073T>C
|
|
|
NR_147928.2:n.2117T>C
|
|
|
NR_147929.2:n.1871T>C
|
|
|