ENST00000502613.3:c.3283C>T
(BMP2K)
MANE Select
|
ENSP00000424668.2:p.His1095Tyr
|
|
ENST00000335016.9:c.3283C>T
(BMP2K)
|
ENSP00000334836.5:p.His1095Tyr
|
|
ENST00000342820.10:c.*782+3380G>A
(PAQR3)
|
ENSP00000344203.6:n.*782+3380G>A
|
|
ENST00000502613.1:c.2360C>T
(BMP2K)
|
|
|
ENST00000511594.5:c.*359G>A
(PAQR3)
|
ENSP00000425080.1:n.*359G>A
|
|
ENST00000512760.5:c.*792+3380G>A
(PAQR3)
|
ENSP00000426875.1:n.*792+3380G>A
|
|
ENST00000628286.1:c.*2259C>T
(BMP2K)
|
ENSP00000487317.1:n.*2259C>T
|
|
NM_198892.1:c.3283C>T
(BMP2K)
|
NP_942595.1:p.His1095Tyr
|
|
XM_005263117.1:c.3172C>T
(BMP2K)
|
XP_005263174.1:p.His1058Tyr
|
|
XM_011532101.1:c.3043C>T
(BMP2K)
|
XP_011530403.1:p.His1015Tyr
|
|
XR_938694.1:n.1118-5669G>A
(PAQR3)
|
|
|
XM_017008381.1:c.3043C>T
(BMP2K)
|
XP_016863870.1:p.His1015Tyr
|
|
XM_017008382.1:c.2395C>T
(BMP2K)
|
XP_016863871.1:p.His799Tyr
|
|
XR_938694.3:n.1098-5669G>A
(PAQR3)
|
|
|
NM_198892.2:c.3283C>T
(BMP2K)
MANE Select
|
NP_942595.1:p.His1095Tyr
|
|