ENST00000617695.5:c.7735C>T
|
ENSP00000481744.2:p.Gln2579Ter
|
|
ENST00000618192.5:c.8011C>T
|
ENSP00000480802.2:p.Gln2671Ter
|
|
ENST00000421865.3:c.7747C>T
MANE Select
|
ENSP00000400365.2:p.Gln2583Ter
|
|
ENST00000421865.2:c.7747C>T
|
ENSP00000400365.2:p.Gln2583Ter
|
|
ENST00000617695.4:c.7735C>T
|
ENSP00000481744.1:p.Gln2579Ter
|
|
ENST00000618192.4:c.7744C>T
|
ENSP00000480802.1:p.Gln2582Ter
|
|
NM_000426.3:c.7747C>T , LRG_409t1:c.7747C>T
|
NP_000417.2:p.Gln2583Ter
|
|
NM_001079823.1:c.7735C>T
|
NP_001073291.1:p.Gln2579Ter
|
|
XM_005266981.2:c.8011C>T
|
XP_005267038.1:p.Gln2671Ter
|
|
XM_005266982.2:c.7999C>T
|
XP_005267039.1:p.Gln2667Ter
|
|
XM_011535820.1:c.8005C>T
|
XP_011534122.1:p.Gln2669Ter
|
|
XM_005266981.3:c.8011C>T
|
XP_005267038.1:p.Gln2671Ter
|
|
XM_005266982.3:c.7999C>T
|
XP_005267039.1:p.Gln2667Ter
|
|
XM_011535820.2:c.8005C>T
|
XP_011534122.1:p.Gln2669Ter
|
|
XM_017010851.2:c.8017C>T
|
XP_016866340.1:p.Gln2673Ter
|
|
XM_017010852.1:c.6142C>T
|
XP_016866341.1:p.Gln2048Ter
|
|
NM_000426.4:c.7747C>T
MANE Select
|
NP_000417.3:p.Gln2583Ter
|
|
NM_001079823.2:c.7735C>T
|
NP_001073291.2:p.Gln2579Ter
|
|