ENST00000502613.3:c.2997C>A
(BMP2K)
MANE Select
|
ENSP00000424668.2:p.Gly999=
|
|
ENST00000335016.9:c.2997C>A
(BMP2K)
|
ENSP00000334836.5:p.Gly999=
|
|
ENST00000342820.10:c.*782+3666G>T
(PAQR3)
|
ENSP00000344203.6:n.*782+3666G>T
|
|
ENST00000502613.1:c.2074C>A
(BMP2K)
|
|
|
ENST00000511594.5:c.*645G>T
(PAQR3)
|
ENSP00000425080.1:n.*645G>T
|
|
ENST00000512760.5:c.*792+3666G>T
(PAQR3)
|
ENSP00000426875.1:n.*792+3666G>T
|
|
ENST00000628286.1:c.*1973C>A
(BMP2K)
|
ENSP00000487317.1:n.*1973C>A
|
|
NM_198892.1:c.2997C>A
(BMP2K)
|
NP_942595.1:p.Gly999=
|
|
XM_005263117.1:c.2886C>A
(BMP2K)
|
XP_005263174.1:p.Gly962=
|
|
XM_011532101.1:c.2757C>A
(BMP2K)
|
XP_011530403.1:p.Gly919=
|
|
XR_938694.1:n.1118-5383G>T
(PAQR3)
|
|
|
XM_017008381.1:c.2757C>A
(BMP2K)
|
XP_016863870.1:p.Gly919=
|
|
XM_017008382.1:c.2109C>A
(BMP2K)
|
XP_016863871.1:p.Gly703=
|
|
XR_938694.3:n.1098-5383G>T
(PAQR3)
|
|
|
NM_198892.2:c.2997C>A
(BMP2K)
MANE Select
|
NP_942595.1:p.Gly999=
|
|