ENST00000383408.7:c.5713G>A
|
ENSP00000372900.4:p.Ala1905Thr
|
|
ENST00000643712.1:c.721G>A
|
ENSP00000493635.1:p.Ala241Thr
|
|
ENST00000674853.1:c.5977G>A
MANE Select
|
ENSP00000501957.1:p.Ala1993Thr
|
|
ENST00000302079.10:c.5638G>A
|
ENSP00000303316.6:p.Ala1880Thr
|
|
ENST00000383408.6:c.5491G>A
|
ENSP00000372900.3:p.Ala1831Thr
|
|
ENST00000503781.7:c.5638G>A
|
ENSP00000421377.3:p.Ala1880Thr
|
|
ENST00000580640.5:c.5713G>A
|
ENSP00000463094.1:p.Ala1905Thr
|
|
ENST00000582913.5:c.5844G>A
|
ENSP00000462115.1:n.5844G>A
|
|
NM_022068.3:c.5638G>A
|
NP_071351.2:p.Ala1880Thr
|
|
XM_011525723.1:c.5770G>A
|
XP_011524025.1:p.Ala1924Thr
|
|
XM_011525724.1:c.5713G>A
|
XP_011524026.1:p.Ala1905Thr
|
|
XM_011525725.1:c.5680G>A
|
XP_011524027.1:p.Ala1894Thr
|
|
XM_011525726.1:c.5770G>A
|
XP_011524028.1:p.Ala1924Thr
|
|
XM_011525723.3:c.5770G>A
|
XP_011524025.1:p.Ala1924Thr
|
|
XM_011525724.3:c.5713G>A
|
XP_011524026.1:p.Ala1905Thr
|
|
XM_011525725.3:c.5680G>A
|
XP_011524027.1:p.Ala1894Thr
|
|
XM_011525726.3:c.5770G>A
|
XP_011524028.1:p.Ala1924Thr
|
|
XM_017025918.2:c.5731G>A
|
XP_016881407.1:p.Ala1911Thr
|
|
XR_001753259.2:n.6767G>A
|
|
|
NM_001378183.1:c.5977G>A
MANE Select
|
NP_001365112.1:p.Ala1993Thr
|
|
NM_022068.4:c.5638G>A
|
NP_071351.2:p.Ala1880Thr
|
|