ENST00000224721.12:c.5613C>G
MANE Select
|
ENSP00000224721.9:p.Ala1871=
|
|
ENST00000224721.10:c.5628C>G
|
ENSP00000224721.8:p.Ala1876=
|
|
ENST00000622827.4:c.5613C>G
|
ENSP00000483211.1:p.Ala1871=
|
|
NM_022124.5:c.5613C>G
|
NP_071407.4:p.Ala1871=
|
|
XM_006717940.2:c.5808C>G
|
XP_006718003.1:p.Ala1936=
|
|
XM_006717942.2:c.5742C>G
|
XP_006718005.1:p.Ala1914=
|
|
XM_011540039.1:c.5805C>G
|
XP_011538341.1:p.Ala1935=
|
|
XM_011540040.1:c.5802C>G
|
XP_011538342.1:p.Ala1934=
|
|
XM_011540041.1:c.5748C>G
|
XP_011538343.1:p.Ala1916=
|
|
XM_011540042.1:c.5808C>G
|
XP_011538344.1:p.Ala1936=
|
|
XM_011540043.1:c.5808C>G
|
XP_011538345.1:p.Ala1936=
|
|
XM_011540044.1:c.5673C>G
|
XP_011538346.1:p.Ala1891=
|
|
XM_011540045.1:c.5808C>G
|
XP_011538347.1:p.Ala1936=
|
|
XM_011540046.1:c.5268C>G
|
XP_011538348.1:p.Ala1756=
|
|
XM_011540047.1:c.4626C>G
|
XP_011538349.1:p.Ala1542=
|
|
XM_011540048.1:c.5808C>G
|
XP_011538350.1:p.Ala1936=
|
|
XM_011540049.1:c.5808C>G
|
XP_011538351.1:p.Ala1936=
|
|
XM_011540050.1:c.5808C>G
|
XP_011538352.1:p.Ala1936=
|
|
XM_011540051.1:c.5808C>G
|
XP_011538353.1:p.Ala1936=
|
|
XM_011540052.1:c.2136C>G
|
XP_011538354.1:p.Ala712=
|
|
XM_011540053.1:c.5808C>G
|
XP_011538355.1:p.Ala1936=
|
|
XR_945796.1:n.6051C>G
|
|
|
NM_022124.6:c.5613C>G
MANE Select
|
NP_071407.4:p.Ala1871=
|
|