ENST00000502613.3:c.3223C>G
(BMP2K)
MANE Select
|
ENSP00000424668.2:p.His1075Asp
|
|
ENST00000335016.9:c.3223C>G
(BMP2K)
|
ENSP00000334836.5:p.His1075Asp
|
|
ENST00000342820.10:c.*782+3440G>C
(PAQR3)
|
ENSP00000344203.6:n.*782+3440G>C
|
|
ENST00000502613.1:c.2300C>G
(BMP2K)
|
|
|
ENST00000511594.5:c.*419G>C
(PAQR3)
|
ENSP00000425080.1:n.*419G>C
|
|
ENST00000512760.5:c.*792+3440G>C
(PAQR3)
|
ENSP00000426875.1:n.*792+3440G>C
|
|
ENST00000628286.1:c.*2199C>G
(BMP2K)
|
ENSP00000487317.1:n.*2199C>G
|
|
NM_198892.1:c.3223C>G
(BMP2K)
|
NP_942595.1:p.His1075Asp
|
|
XM_005263117.1:c.3112C>G
(BMP2K)
|
XP_005263174.1:p.His1038Asp
|
|
XM_011532101.1:c.2983C>G
(BMP2K)
|
XP_011530403.1:p.His995Asp
|
|
XR_938694.1:n.1118-5609G>C
(PAQR3)
|
|
|
XM_017008381.1:c.2983C>G
(BMP2K)
|
XP_016863870.1:p.His995Asp
|
|
XM_017008382.1:c.2335C>G
(BMP2K)
|
XP_016863871.1:p.His779Asp
|
|
XR_938694.3:n.1098-5609G>C
(PAQR3)
|
|
|
NM_198892.2:c.3223C>G
(BMP2K)
MANE Select
|
NP_942595.1:p.His1075Asp
|
|